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: rs9034
rs9034
0.827 0.200 7 106249610 3 prime UTR variant A/G;T snv
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic
Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs9034
rs9034
0.827 0.200 7 106249610 3 prime UTR variant A/G;T snv
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2014 2014
dbSNP: rs9034
rs9034
0.827 0.200 7 106249610 3 prime UTR variant A/G;T snv
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2014 2014
dbSNP: rs9034
rs9034
0.827 0.200 7 106249610 3 prime UTR variant A/G;T snv
Squamous cell carcinoma of esophagus
Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs9034
rs9034
0.827 0.200 7 106249610 3 prime UTR variant A/G;T snv
Malignant neoplasm of urinary bladder
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2014 2014
dbSNP: rs16872158
rs16872158
0.925 0.040 7 106265839 intron variant T/A snv 1.6E-03
CUI: C1384584
Disease: Generalized osteoarthritis
Generalized osteoarthritis
Musculoskeletal Diseases 0.010 1.000 1 2016 2016
dbSNP: rs16872158
rs16872158
0.925 0.040 7 106265839 intron variant T/A snv 1.6E-03
CUI: C0409952
Disease: Idiopathic osteoarthritis
Idiopathic osteoarthritis
Musculoskeletal Diseases 0.010 1.000 1 2016 2016
dbSNP: rs10487818
rs10487818
1.000 0.080 7 106269615 intron variant A/T snv 1.1E-02
CUI: C0028756
Disease: Obesity, Morbid
Obesity, Morbid
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2009 2009
dbSNP: rs10271556
rs10271556
7 106258428 intron variant C/T snv 5.6E-02
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs10271556
rs10271556
7 106258428 intron variant C/T snv 5.6E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs10271556
rs10271556
7 106258428 intron variant C/T snv 5.6E-02
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs10271556
rs10271556
7 106258428 intron variant C/T snv 5.6E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs59744560
rs59744560
1.000 0.120 7 106285832 5 prime UTR variant C/A snv 9.5E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs61330082
rs61330082
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs61330082
rs61330082
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22
Malignant neoplasm of urinary bladder
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2014 2014
dbSNP: rs61330082
rs61330082
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22
Respiratory Distress Syndrome, Adult
Respiratory Tract Diseases 0.010 1.000 1 2012 2012
dbSNP: rs61330082
rs61330082
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs61330082
rs61330082
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22
CUI: C0036690
Disease: Septicemia
Septicemia
Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2012 2012
dbSNP: rs61330082
rs61330082
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs61330082
rs61330082
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2014 2014
dbSNP: rs61330082
rs61330082
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22
CUI: C0243026
Disease: Sepsis
Sepsis
Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2012 2012
dbSNP: rs61330082
rs61330082
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic
Digestive System Diseases; Infections 0.010 1.000 1 2016 2016
dbSNP: rs61330082
rs61330082
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22
CUI: C0004626
Disease: Pneumonia, Bacterial
Pneumonia, Bacterial
Infections; Respiratory Tract Diseases 0.010 1.000 1 2012 2012
dbSNP: rs61330082
rs61330082
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22
Squamous cell carcinoma of esophagus
Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs61330082
rs61330082
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic
Cardiovascular Diseases 0.010 1.000 1 2015 2015