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: rs7665590
rs7665590 		0.925 0.080 4 98875633 3 prime UTR variant T/C snv 0.56
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.800 1.000 1 2012 2012
dbSNP: rs199646819
rs199646819 		4 98927473 intron variant TGG/- delins 8.2E-02
CUI: C1629609
Disease: Age at menopause
Age at menopause 		0.700 1.000 1 2018 2018
dbSNP: rs62323189
rs62323189 		4 98874312 3 prime UTR variant T/C snv 0.26
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs7665590
rs7665590 		0.925 0.080 4 98875633 3 prime UTR variant T/C snv 0.56
CUI: C0023892
Disease: Biliary cirrhosis
Biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs1363867515
rs1363867515 		1.000 0.080 4 98901908 synonymous variant T/C snv 1.2E-05
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		Nutritional and Metabolic Diseases; Nervous System Diseases 0.010 1.000 1 2003 2003