Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3939286
rs3939286 		0.776 0.360 9 6210099 regulatory region variant T/A;C snv
CUI: C0004096
Disease: Asthma
Asthma 		0.710 1.000 2 2010 2020
dbSNP: rs3939286
rs3939286 		0.776 0.360 9 6210099 regulatory region variant T/A;C snv
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs3939286
rs3939286 		0.776 0.360 9 6210099 regulatory region variant T/A;C snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2013 2013
dbSNP: rs3939286
rs3939286 		0.776 0.360 9 6210099 regulatory region variant T/A;C snv
CUI: C1306759
Disease: Eosinophilic disorder
Eosinophilic disorder 		0.010 1.000 1 2010 2010
dbSNP: rs3939286
rs3939286 		0.776 0.360 9 6210099 regulatory region variant T/A;C snv
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.010 1.000 1 2015 2015
dbSNP: rs3939286
rs3939286 		0.776 0.360 9 6210099 regulatory region variant T/A;C snv
CUI: C0027430
Disease: Nasal Polyps
Nasal Polyps 		0.010 1.000 1 2010 2010
dbSNP: rs3939286
rs3939286 		0.776 0.360 9 6210099 regulatory region variant T/A;C snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.010 1.000 1 2013 2013
dbSNP: rs3939286
rs3939286 		0.776 0.360 9 6210099 regulatory region variant T/A;C snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.010 1.000 1 2015 2015
dbSNP: rs3939286
rs3939286 		0.776 0.360 9 6210099 regulatory region variant T/A;C snv
CUI: C0014457
Disease: Eosinophilia
Eosinophilia 		0.010 1.000 1 2010 2010
dbSNP: rs3939286
rs3939286 		0.776 0.360 9 6210099 regulatory region variant T/A;C snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.010 1.000 1 2013 2013
dbSNP: rs3939286
rs3939286 		0.776 0.360 9 6210099 regulatory region variant T/A;C snv
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.010 1.000 1 2015 2015
dbSNP: rs3939286
rs3939286 		0.776 0.360 9 6210099 regulatory region variant T/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2013 2013