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: rs2301220
rs2301220 		1.000 0.080 6 33070989 intron variant C/A;T snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 3 2009 2013
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: rs1431399
rs1431399 		1.000 0.080 6 33073257 intron variant A/G;T snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 2 2011 2013
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: 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: 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: rs10214910
rs10214910 		1.000 0.080 6 33069898 intron variant C/A snv 0.23 0.32
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs13213149
rs13213149 		1.000 0.080 6 33071909 intron variant T/C snv 0.28
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs1431400
rs1431400 		1.000 0.080 6 33073399 intron variant C/T snv 0.29
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs1431401
rs1431401 		1.000 0.080 6 33073409 intron variant G/A snv 0.29
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs1431403
rs1431403 		0.925 0.200 6 33079254 intron variant T/C snv 0.37
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: rs2021408
rs2021408 		1.000 0.040 6 33078949 intron variant T/C snv 0.15
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer 		Stomatognathic Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2071349
rs2071349 		1.000 0.080 6 33075743 intron variant C/G snv 0.14
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs2071351
rs2071351 		1.000 0.080 6 33076153 intron variant A/G snv 0.24 0.29
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs2071353
rs2071353 		1.000 0.080 6 33076480 intron variant T/C;G snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs2301224
rs2301224 		1.000 0.080 6 33070592 intron variant C/A snv 0.28
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs2567279
rs2567279 		1.000 0.080 6 33078885 intron variant T/C snv 0.27
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs28452918
rs28452918 		1.000 0.080 6 33071518 intron variant T/A snv 0.29
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs2856821
rs2856821 		1.000 0.040 6 33078965 intron variant T/C snv 0.21
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		Musculoskeletal Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2856830
rs2856830 		0.925 0.080 6 33073957 intron variant T/C snv 0.12
CUI: C2973725
Disease: Pulmonary arterial hypertension
Pulmonary arterial hypertension 		Respiratory Tract Diseases; Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2856830
rs2856830 		0.925 0.080 6 33073957 intron variant T/C snv 0.12
CUI: C1701938
Disease: Associated Pulmonary Arterial Hypertension
Associated Pulmonary Arterial Hypertension 		Respiratory Tract Diseases 0.010 1.000 1 2019 2019
dbSNP: rs3097670
rs3097670 		6 33078975 intron variant G/A;C snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs3135021
rs3135021 		0.925 0.080 6 33077781 intron variant G/A snv 0.32
CUI: C4075603
Disease: Occult chronic type B viral hepatitis
Occult chronic type B viral hepatitis 		Digestive System Diseases; Infections 0.010 1.000 1 2017 2017
dbSNP: rs4640928
rs4640928 		1.000 0.080 6 33072819 intron variant A/G snv 0.29
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs6914849
rs6914849 		1.000 0.080 6 33072938 intron variant G/A snv 0.28
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013