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: rs7303112
rs7303112 		12 98678114 intron variant C/T snv 3.0E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs117235991
rs117235991 		1.000 0.040 12 98699448 missense variant A/C snv 9.5E-03 7.8E-03
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs138526583
rs138526583 		1.000 0.040 12 98699432 missense variant G/A snv 3.4E-03 3.1E-03
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs141157255
rs141157255 		0.882 0.120 12 98659331 missense variant G/A snv 4.0E-05 2.8E-05
CUI: C1739405
Disease: CML progression
CML progression 		0.010 1.000 1 2007 2007
dbSNP: rs141157255
rs141157255 		0.882 0.120 12 98659331 missense variant G/A snv 4.0E-05 2.8E-05
CUI: C0005699
Disease: Blast Phase
Blast Phase 		Pathological Conditions, Signs and Symptoms; Neoplasms; Hemic and Lymphatic Diseases 0.010 1.000 1 2007 2007
dbSNP: rs141157255
rs141157255 		0.882 0.120 12 98659331 missense variant G/A snv 4.0E-05 2.8E-05
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic 		Neoplasms; Hemic and Lymphatic Diseases 0.010 1.000 1 2007 2007
dbSNP: rs1476273292
rs1476273292 		1.000 0.040 12 98712328 missense variant G/A snv 4.0E-06
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.010 1.000 1 2002 2002
dbSNP: rs746482334
rs746482334 		1.000 0.040 12 98732507 missense variant A/G snv 4.0E-06
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.010 < 0.001 1 2003 2003