Source: CURATED ×
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: rs2516049
rs2516049
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 4 2007 2011
dbSNP: rs660895
rs660895
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.810 1.000 3 2007 2018
dbSNP: rs615672
rs615672
0.851 0.240 6 32606394 intergenic variant G/A;C snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.800 1.000 2 2007 2011
dbSNP: rs9270657
rs9270657
0.925 0.160 6 32598244 intergenic variant T/G snv 0.42
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs477515
rs477515
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27
CUI: C1956391
Disease: Temporal Arteritis
Temporal Arteritis
Skin and Connective Tissue Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2015 2015
dbSNP: rs9271100
rs9271100
0.925 0.120 6 32608701 regulatory region variant T/A;C snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.800 1.000 2 2009 2013
dbSNP: rs2516049
rs2516049
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0030809
Disease: Pemphigus Vulgaris
Pemphigus Vulgaris
Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs660895
rs660895
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19
CUI: C0030809
Disease: Pemphigus Vulgaris
Pemphigus Vulgaris
Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs660895
rs660895
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs9270984
rs9270984
1.000 0.080 6 32606214 intergenic variant T/A;G snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.800 1.000 1 2013 2013
dbSNP: rs9271055
rs9271055
1.000 0.080 6 32607592 intergenic variant G/T snv 0.84
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs532098
rs532098
0.882 0.120 6 32610275 intergenic variant G/A snv 0.43
CUI: C0042900
Disease: Vitiligo
Vitiligo
Skin and Connective Tissue Diseases 0.700 1.000 2 2010 2012
dbSNP: rs2516049
rs2516049
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0042900
Disease: Vitiligo
Vitiligo
Skin and Connective Tissue Diseases 0.700 1.000 1 2010 2010
dbSNP: rs2858870
rs2858870
0.851 0.280 6 32604474 intergenic variant T/A;C snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
Skin and Connective Tissue Diseases 0.700 1.000 1 2010 2010
dbSNP: rs1064713
rs1064713
1.000 0.080 6 32578889 3 prime UTR variant G/A;C;T snv 2.6E-02 2.1E-02
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs545366210
rs545366210
1.000 0.080 6 32586302 intron variant T/C snv
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs7760841
rs7760841
1.000 0.080 6 32607091 intergenic variant C/T snv 0.14
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2760995
rs2760995
6 32606581 intergenic variant G/A snv 0.20
CUI: C0730345
Disease: Microalbuminuria
Microalbuminuria
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2516049
rs2516049
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs2858870
rs2858870
0.851 0.280 6 32604474 intergenic variant T/A;C snv
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs477515
rs477515
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs601945
rs601945
1.000 0.120 6 32605638 intergenic variant A/G snv 0.13
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs660895
rs660895
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs615672
rs615672
0.851 0.240 6 32606394 intergenic variant G/A;C snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs9269853
rs9269853
1.000 0.080 6 32582545 intron variant A/C;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.700 1.000 1 2019 2019