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: rs3077
rs3077
0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
Digestive System Diseases; Infections 0.900 0.913 23 2009 2019
dbSNP: rs3077
rs3077
0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29
CUI: C0524909
Disease: Hepatitis B, Chronic
Hepatitis B, Chronic
Digestive System Diseases; Infections 0.760 1.000 8 2011 2017
dbSNP: rs3077
rs3077
0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.740 0.600 5 2011 2015
dbSNP: rs3077
rs3077
0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.050 0.600 5 2011 2014
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: rs3077
rs3077
0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29
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: 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: 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: rs9469341
rs9469341
1.000 0.080 6 33068100 3 prime UTR variant A/C;G snv
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: rs111789468
rs111789468
1.000 0.080 6 33066047 non coding transcript exon variant C/T snv 0.21
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs116722486
rs116722486
6 33080823 synonymous variant T/C;G snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2018 2018
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: rs1367728
rs1367728
1.000 0.120 6 33067038 non coding transcript exon variant G/A snv 0.10
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2007 2007
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: rs17214519
rs17214519
1.000 0.080 6 33064411 downstream gene variant G/A;T snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
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: 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