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: rs1063355
rs1063355 		0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		Eye Diseases 0.010 1.000 1 2017 2017
dbSNP: rs41563814
rs41563814 		1.000 0.040 6 32664881 missense variant A/T snv 3.2E-05
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		Eye Diseases 0.010 1.000 1 2016 2016
dbSNP: rs9274390
rs9274390 		0.925 0.080 6 32664882 missense variant C/G;T snv 3.9E-02
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		Eye Diseases 0.010 1.000 1 2016 2016
dbSNP: rs3891175
rs3891175 		0.851 0.160 6 32666690 5 prime UTR variant C/T snv 0.20
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs2854275
rs2854275 		0.925 0.120 6 32660651 non coding transcript exon variant C/A snv 9.6E-02
CUI: C0201278
Disease: Antibody measurement (procedure)
Antibody measurement (procedure) 		0.700 1.000 1 2013 2013
dbSNP: rs28724231
rs28724231 		1.000 0.080 6 32659314 upstream gene variant A/G snv 2.9E-02
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1063355
rs1063355 		0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs201184533
rs201184533 		1.000 0.080 6 32665110 intron variant C/A;T snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2854275
rs2854275 		0.925 0.120 6 32660651 non coding transcript exon variant C/A snv 9.6E-02
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs9273410
rs9273410 		1.000 0.080 6 32659473 3 prime UTR variant C/A snv 0.51
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs9274659
rs9274659 		1.000 0.080 6 32668608 upstream gene variant A/G;T snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs3891175
rs3891175 		0.851 0.160 6 32666690 5 prime UTR variant C/T snv 0.20
CUI: C0241910
Disease: Autoimmune Chronic Hepatitis
Autoimmune Chronic Hepatitis 		Digestive System Diseases; Immune System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs3891175
rs3891175 		0.851 0.160 6 32666690 5 prime UTR variant C/T snv 0.20
CUI: C1332355
Disease: Autoimmune Hepatitis with Centrilobular Necrosis
Autoimmune Hepatitis with Centrilobular Necrosis 		0.700 1.000 1 2018 2018
dbSNP: rs281862010
rs281862010 		6 32665113 intron variant C/A;G snv 1.5E-05
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4713572
rs4713572 		6 32659175 upstream gene variant T/A;C snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs9273552
rs9273552 		6 32661139 intron variant G/A snv 1.8E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs9274407
rs9274407 		0.925 0.120 6 32665055 missense variant A/C;T snv 0.77
CUI: C4277682
Disease: Chemical and Drug Induced Liver Injury
Chemical and Drug Induced Liver Injury 		Digestive System Diseases; Chemically-Induced Disorders 0.800 1.000 1 2011 2011
dbSNP: rs9274299
rs9274299 		1.000 0.040 6 32664181 non coding transcript exon variant C/A;G;T snv 1.7E-03
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs9274390
rs9274390 		0.925 0.080 6 32664882 missense variant C/G;T snv 3.9E-02
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs9274657
rs9274657 		1.000 0.040 6 32668587 upstream gene variant G/A snv 0.37
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs3891175
rs3891175 		0.851 0.160 6 32666690 5 prime UTR variant C/T snv 0.20
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		Digestive System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs9273404
rs9273404 		1.000 0.040 6 32659383 upstream gene variant A/G snv 0.56
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1063355
rs1063355 		0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs9273643
rs9273643 		0.925 0.120 6 32661407 missense variant A/G snv
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.010 1.000 1 2000 2000
dbSNP: rs9273643
rs9273643 		0.925 0.120 6 32661407 missense variant A/G snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2000 2000