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: rs3740835
rs3740835 		1.000 0.040 11 128900463 3 prime UTR variant G/A;T snv
CUI: C1384514
Disease: Conn Syndrome
Conn Syndrome 		Endocrine System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs6590357
rs6590357 		0.882 0.120 11 128911444 synonymous variant T/C snv 0.84 0.85
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs6590357
rs6590357 		0.882 0.120 11 128911444 synonymous variant T/C snv 0.84 0.85
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs6590357
rs6590357 		0.882 0.120 11 128911444 synonymous variant T/C snv 0.84 0.85
CUI: C0340489
Disease: Lone atrial fibrillation
Lone atrial fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2011 2011