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: rs12721627
rs12721627 		7 99768470 missense variant G/C snv 7.6E-05 5.6E-05
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2006 2006
dbSNP: rs12721627
rs12721627 		7 99768470 missense variant G/C snv 7.6E-05 5.6E-05
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2006 2006
dbSNP: rs138105638
rs138105638 		7 99766440 stop gained G/A;T snv 6.4E-05 7.7E-05
CUI: C0030193
Disease: Pain
Pain 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2018 2018
dbSNP: rs138105638
rs138105638 		7 99766440 stop gained G/A;T snv 6.4E-05 7.7E-05
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs138105638
rs138105638 		7 99766440 stop gained G/A;T snv 6.4E-05 7.7E-05
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs34642455
rs34642455 		7 99777087 intron variant T/C snv 8.8E-03
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs3735451
rs3735451 		7 99758352 intron variant T/C snv 0.31
CUI: C1510472
Disease: Drug Dependence
Drug Dependence 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs4646440
rs4646440 		7 99763247 intron variant G/A snv 5.1E-02
CUI: C0087169
Disease: Withdrawal Symptoms
Withdrawal Symptoms 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs4646440
rs4646440 		7 99763247 intron variant G/A snv 5.1E-02
CUI: C1510472
Disease: Drug Dependence
Drug Dependence 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs2740574
rs2740574 		0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.020 1.000 2 2013 2014
dbSNP: rs2740574
rs2740574 		0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.020 1.000 2 2013 2014
dbSNP: rs2740574
rs2740574 		0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 < 0.001 1 2010 2010
dbSNP: rs2740574
rs2740574 		0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs2740574
rs2740574 		0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78
CUI: C0565599
Disease: Maternal hypertension
Maternal hypertension 		Female Urogenital Diseases and Pregnancy Complications; Cardiovascular Diseases 0.010 < 0.001 1 2010 2010
dbSNP: rs2740574
rs2740574 		0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2009 2009
dbSNP: rs2740574
rs2740574 		0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78
CUI: C0852036
Disease: Pregnancy associated hypertension
Pregnancy associated hypertension 		Female Urogenital Diseases and Pregnancy Complications; Cardiovascular Diseases 0.010 < 0.001 1 2010 2010
dbSNP: rs2740574
rs2740574 		0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs2740574
rs2740574 		0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78
CUI: C0024312
Disease: Lymphopenia
Lymphopenia 		Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2740574
rs2740574 		0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78
CUI: C0002170
Disease: Alopecia
Alopecia 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2740574
rs2740574 		0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs2740574
rs2740574 		0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78
CUI: C0041912
Disease: Upper Respiratory Infections
Upper Respiratory Infections 		Infections; Respiratory Tract Diseases 0.010 1.000 1 2018 2018
dbSNP: rs4646437
rs4646437 		0.827 0.200 7 99767460 intron variant G/A snv 0.30
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.020 1.000 2 2017 2019
dbSNP: rs4646437
rs4646437 		0.827 0.200 7 99767460 intron variant G/A snv 0.30
CUI: C0015672
Disease: Fatigue
Fatigue 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2017 2017
dbSNP: rs4646437
rs4646437 		0.827 0.200 7 99767460 intron variant G/A snv 0.30
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs4646437
rs4646437 		0.827 0.200 7 99767460 intron variant G/A snv 0.30
CUI: C1510472
Disease: Drug Dependence
Drug Dependence 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2019 2019