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: 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: 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
CUI: C1275122
Disease: Familial multiple trichoepitheliomata
Familial multiple trichoepitheliomata 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2013 2013
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: rs2023463
rs2023463 		1.000 0.040 6 29445226 intron variant C/T snv 7.6E-02
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2023463
rs2023463 		1.000 0.040 6 29445226 intron variant C/T snv 7.6E-02
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs2023463
rs2023463 		1.000 0.040 6 29445226 intron variant C/T snv 7.6E-02
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2019 2019
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: 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: 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: rs238883
rs238883 		6 29378449 intron variant G/A snv 0.59
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs3117440
rs3117440 		6 29373889 3 prime UTR variant T/A snv 0.95
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs3129685
rs3129685 		6 29357825 intron variant G/A snv 0.95
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs3129684
rs3129684 		6 29357383 intron variant G/C snv 0.95
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012