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: rs11700980
rs11700980 		21 28781917 regulatory region variant T/C snv 8.7E-02
CUI: C0429097
Disease: QRS complex feature
QRS complex feature 		0.700 1.000 1 2016 2016
dbSNP: rs1997606
rs1997606 		21 28885238 synonymous variant C/A;G snv 0.84
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs2409317
rs2409317 		1.000 0.080 21 28702102 intergenic variant C/T snv 0.97
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2016 2016
dbSNP: rs56923832
rs56923832 		21 28663270 intron variant T/A snv 0.15
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs73186036
rs73186036 		21 28754160 regulatory region variant A/G snv 0.20
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.700 1.000 1 2018 2018
dbSNP: rs73186036
rs73186036 		21 28754160 regulatory region variant A/G snv 0.20
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2254638
rs2254638 		0.882 0.040 21 28883961 intron variant A/C;G snv
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.020 1.000 2 2017 2018
dbSNP: rs2254638
rs2254638 		0.882 0.040 21 28883961 intron variant A/C;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.020 1.000 2 2017 2018
dbSNP: rs2254638
rs2254638 		0.882 0.040 21 28883961 intron variant A/C;G snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.020 1.000 2 2017 2018