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: rs429479
rs429479
6 29404546 intron variant A/G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs429479
rs429479
6 29404546 intron variant A/G;T snv
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 1.000 1 2019 2019
dbSNP: rs4713211
rs4713211
1.000 0.120 6 29368277 intron variant G/A snv 0.59
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2009 2009
dbSNP: rs7753474
rs7753474
1.000 0.120 6 29373531 3 prime UTR variant G/A snv 0.22
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2009 2009
dbSNP: rs7761746
rs7761746
6 29355878 missense variant G/A;T snv 3.0E-02 7.1E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs9257802
rs9257802
6 29375578 intron variant C/T snv 0.20
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs9257809
rs9257809
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs9257809
rs9257809
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs9257809
rs9257809
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure
0.700 1.000 1 2012 2012
dbSNP: rs9257809
rs9257809
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
Adenocarcinoma Of Esophagus
Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs9257809
rs9257809
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
Hemic and Lymphatic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs9257809
rs9257809
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index
0.700 1.000 1 2012 2012
dbSNP: rs545611345
rs545611345
1.000 0.080 6 29374540 missense variant A/G snv 1.2E-05
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs9257809
rs9257809
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease
Digestive System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs9257809
rs9257809
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02
CUI: C0018834
Disease: Heartburn
Heartburn
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2017 2017
dbSNP: rs9257809
rs9257809
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02
Familial multiple trichoepitheliomata
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2013 2013