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: 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: 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: 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: 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: rs3077
rs3077 		0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29
CUI: C0262988
Disease: Vasculitis of the skin
Vasculitis of the skin 		Skin and Connective Tissue Diseases; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3077
rs3077 		0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29
CUI: C0014060
Disease: Encephalitis, St. Louis
Encephalitis, St. Louis 		Infections; Nervous System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3077
rs3077 		0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2013 2013
dbSNP: rs3077
rs3077 		0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29
CUI: C4048328
Disease: cervical cancer
cervical cancer 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2013 2013
dbSNP: rs3077
rs3077 		0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2013 2013
dbSNP: rs3077
rs3077 		0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.010 1.000 1 2014 2014
dbSNP: rs3077
rs3077 		0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29
CUI: C1623038
Disease: Cirrhosis
Cirrhosis 		Pathological Conditions, Signs and Symptoms 0.010 < 0.001 1 2011 2011
dbSNP: rs3077
rs3077 		0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs3077
rs3077 		0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3077
rs3077 		0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29
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: rs3077
rs3077 		0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs3179779
rs3179779 		1.000 0.080 6 33068192 3 prime UTR variant A/C;G snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs3180553
rs3180553 		1.000 0.080 6 33068433 3 prime UTR variant G/T snv 0.32
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs3180554
rs3180554 		1.000 0.080 6 33068400 3 prime UTR variant A/G snv 0.32
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
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: 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: 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: rs1367728
rs1367728 		1.000 0.120 6 33067038 non coding transcript exon variant G/A snv 0.10
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2007 2007