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: rs2012809
rs2012809 		1.000 0.080 5 128854670 intron variant A/G snv 0.86
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 2 2018 2018
dbSNP: rs147450666
rs147450666 		5 128619201 intron variant G/A;T snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs147450666
rs147450666 		5 128619201 intron variant G/A;T snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs35079125
rs35079125 		5 128540536 5 prime UTR variant G/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2019 2019
dbSNP: rs77884860
rs77884860 		5 128873760 intron variant C/T snv 1.1E-02
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs77884860
rs77884860 		5 128873760 intron variant C/T snv 1.1E-02
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs2526246
rs2526246 		1.000 0.040 5 128966131 5 prime UTR variant T/A snv 0.28 0.29
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.010 1.000 1 2012 2012