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: rs9277535
rs9277535 		0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.900 0.917 24 2009 2018
dbSNP: rs987870
rs987870 		0.851 0.160 6 33075103 intron variant A/G snv 0.19
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.810 1.000 1 2011 2011
dbSNP: rs9277554
rs9277554 		0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38
CUI: C3495801
Disease: Granulomatosis with polyangiitis
Granulomatosis with polyangiitis 		Respiratory Tract Diseases; Immune System Diseases; Cardiovascular Diseases 0.800 1.000 1 2013 2013
dbSNP: rs987870
rs987870 		0.851 0.160 6 33075103 intron variant A/G snv 0.19
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.800 1.000 1 2011 2011
dbSNP: rs9277535
rs9277535 		0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic 		Digestive System Diseases; Infections 0.760 1.000 8 2011 2017
dbSNP: rs9277535
rs9277535 		0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.740 0.800 5 2012 2015
dbSNP: rs9277535
rs9277535 		0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25
CUI: C4048328
Disease: cervical cancer
cervical cancer 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.720 1.000 3 2013 2018
dbSNP: rs1042169
rs1042169 		1.000 0.080 6 33080909 missense variant G/A;T snv 0.31; 1.4E-02
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.710 1.000 3 2013 2019
dbSNP: rs3135021
rs3135021 		0.925 0.080 6 33077781 intron variant G/A snv 0.32
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.710 0.667 3 2009 2016
dbSNP: rs9277535
rs9277535 		0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.710 1.000 3 2007 2018
dbSNP: rs9277542
rs9277542 		0.851 0.280 6 33087470 3 prime UTR variant T/A;C snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.710 1.000 3 2012 2016
dbSNP: rs7770370
rs7770370 		0.925 0.160 6 33081144 non coding transcript exon variant A/G snv 0.27
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.710 1.000 2 2013 2015
dbSNP: rs9277378
rs9277378 		0.827 0.320 6 33082502 intron variant A/G snv 0.40
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.710 1.000 2 2013 2013
dbSNP: rs9277471
rs9277471 		1.000 0.080 6 33085905 missense variant G/A;C snv 0.32; 4.1E-06
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.710 1.000 2 2013 2016
dbSNP: rs9277534
rs9277534 		0.790 0.280 6 33087030 3 prime UTR variant A/G snv 0.38
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.710 0.500 2 2013 2018
dbSNP: rs3128965
rs3128965 		0.882 0.280 6 33088122 3 prime UTR variant G/A snv 0.14
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		Skin and Connective Tissue Diseases 0.710 1.000 1 2009 2009
dbSNP: rs7750458
rs7750458 		0.925 0.120 6 33077921 intron variant G/A snv 9.5E-02
CUI: C0011633
Disease: Dermatomyositis
Dermatomyositis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases 0.710 1.000 1 2016 2016
dbSNP: rs9277554
rs9277554 		0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 3 2007 2011
dbSNP: rs1431403
rs1431403 		0.925 0.200 6 33079254 intron variant T/C snv 0.37
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 2 2012 2013
dbSNP: rs553665868
rs553665868 		1.000 0.080 6 33080917 missense variant A/G snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 2 2013 2013
dbSNP: rs9277554
rs9277554 		0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 2 2011 2013
dbSNP: rs987870
rs987870 		0.851 0.160 6 33075103 intron variant A/G snv 0.19
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 2 2007 2009
dbSNP: rs1042133
rs1042133 		6 33080829 missense variant G/C snv 0.14 0.15
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs1042133
rs1042133 		6 33080829 missense variant G/C snv 0.14 0.15
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs1042151
rs1042151 		0.925 0.240 6 33080884 missense variant A/G snv 0.18 0.25
CUI: C1319853
Disease: Asthma, Aspirin-Induced
Asthma, Aspirin-Induced 		Respiratory Tract Diseases; Immune System Diseases; Chemically-Induced Disorders 0.700 1.000 1 2013 2013