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: rs3934467
rs3934467 		1 162212887 intron variant C/T snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 4 2012 2019
dbSNP: rs10494366
rs10494366 		0.851 0.200 1 162115895 intron variant G/T snv 0.54
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 3 2006 2019
dbSNP: rs12029454
rs12029454 		1 162163327 intron variant G/A snv 0.21
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 3 2009 2019
dbSNP: rs12742393
rs12742393 		0.925 0.120 1 162254796 intron variant A/C;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.030 1.000 3 2010 2019
dbSNP: rs16857031
rs16857031 		1 162143120 intron variant C/G snv 0.18
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 3 2009 2019
dbSNP: rs4657175
rs4657175 		1.000 0.040 1 162225948 intron variant T/C;G snv
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 3 2012 2019
dbSNP: rs10494366
rs10494366 		0.851 0.200 1 162115895 intron variant G/T snv 0.54
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 1.000 2 2010 2019
dbSNP: rs10494366
rs10494366 		0.851 0.200 1 162115895 intron variant G/T snv 0.54
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 1.000 2 2010 2010
dbSNP: rs12742393
rs12742393 		0.925 0.120 1 162254796 intron variant A/C;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.020 1.000 2 2009 2018
dbSNP: rs1415259
rs1415259 		0.925 0.080 1 162115519 intron variant C/T snv 0.54
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 2 2010 2019
dbSNP: rs4657172
rs4657172 		1 162209842 intron variant C/G snv 0.82
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 2 2014 2019
dbSNP: rs4657178
rs4657178 		1 162240820 intron variant C/A;G;T snv 0.31
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 2 2009 2019
dbSNP: rs10127719
rs10127719 		1 162186380 intron variant T/A;C snv
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs10494366
rs10494366 		0.851 0.200 1 162115895 intron variant G/T snv 0.54
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs10494366
rs10494366 		0.851 0.200 1 162115895 intron variant G/T snv 0.54
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2009 2009
dbSNP: rs10494366
rs10494366 		0.851 0.200 1 162115895 intron variant G/T snv 0.54
CUI: C0741923
Disease: cardiac event
cardiac event 		0.010 1.000 1 2010 2010
dbSNP: rs10494366
rs10494366 		0.851 0.200 1 162115895 intron variant G/T snv 0.54
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs10800352
rs10800352 		1 162202899 intron variant A/G snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs10800397
rs10800397 		1.000 0.120 1 162267300 intron variant C/G;T snv
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome 		Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs10918602
rs10918602 		1 162067910 upstream gene variant T/C snv 0.25
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs10918796
rs10918796 		1 162163553 intron variant C/A;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs10918859
rs10918859 		0.882 0.040 1 162199478 intron variant G/A snv 0.16
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs10918859
rs10918859 		0.882 0.040 1 162199478 intron variant G/A snv 0.16
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs10918859
rs10918859 		0.882 0.040 1 162199478 intron variant G/A snv 0.16
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs10919021
rs10919021 		1 162265600 intron variant C/T snv 0.97
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012