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: rs6929846
rs6929846
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.780 1.000 8 2011 2014
dbSNP: rs2273558
rs2273558
6 26465807 intron variant A/C;G snv
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 2 2018 2019
dbSNP: rs13195401
rs13195401
1.000 0.080 6 26463346 stop gained G/A;T snv 4.5E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs13195509
rs13195509
1.000 0.080 6 26463432 missense variant G/A snv 5.7E-02 6.4E-02
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 1 2014 2014
dbSNP: rs1977199
rs1977199
1.000 0.040 6 26466161 intron variant G/A snv 0.67
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs1977199
rs1977199
1.000 0.040 6 26466161 intron variant G/A snv 0.67
Child Development Disorders, Pervasive
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs1977200
rs1977200
6 26466164 intron variant G/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs3734542
rs3734542
1.000 0.080 6 26468098 missense variant G/A;C snv 5.8E-02 6.4E-02
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.700 1.000 1 2017 2017
dbSNP: rs3799380
rs3799380
1.000 0.040 6 26466954 intron variant T/C snv 0.31
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs7763910
rs7763910
1.000 0.040 6 26472427 intron variant A/G snv 0.48
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease
Digestive System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs6929846
rs6929846
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.030 1.000 3 2011 2014
dbSNP: rs6929846
rs6929846
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.030 1.000 3 2011 2015
dbSNP: rs6929846
rs6929846
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.030 1.000 3 2011 2015
dbSNP: rs6929846
rs6929846
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
Nutritional and Metabolic Diseases 0.020 1.000 2 2011 2012
dbSNP: rs6929846
rs6929846
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias
Nutritional and Metabolic Diseases 0.020 1.000 2 2012 2014
dbSNP: rs6929846
rs6929846
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70
CUI: C2242712
Disease: Hyper LDL cholesterolaemia
Hyper LDL cholesterolaemia
0.010 1.000 1 2015 2015
dbSNP: rs6929846
rs6929846
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70
CUI: C0011847
Disease: Diabetes
Diabetes
Endocrine System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs6929846
rs6929846
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
Nutritional and Metabolic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs6929846
rs6929846
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2011 2011