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: rs220721
rs220721 		1.000 0.080 6 159907588 synonymous variant C/T snv 0.29 0.27
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs220733
rs220733 		1.000 0.080 6 159897771 intron variant A/C;G snv 0.99
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs220733
rs220733 		1.000 0.080 6 159897771 intron variant A/C;G snv 0.99
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs220733
rs220733 		1.000 0.080 6 159897771 intron variant A/C;G snv 0.99
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs755508039
rs755508039 		1.000 0.040 6 159907236 missense variant A/C;G snv
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		Infections 0.010 1.000 1 2018 2018