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: 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: rs2301226
rs2301226 		1.000 0.080 6 33066819 non coding transcript exon variant G/A snv 0.16
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2011 2011
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: rs2856822
rs2856822 		1.000 0.080 6 33079655 non coding transcript exon variant A/C snv 0.41
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
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: 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: 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: 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: rs36081724
rs36081724 		1.000 0.080 6 33069488 non coding transcript exon variant C/A snv 0.29
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013