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: rs1042140
rs1042140 		1.000 0.120 6 33080863 stop gained A/C;G;T snv 2.4E-05; 0.25
CUI: C4016208
Disease: BERYLLIUM DISEASE, CHRONIC, SUSCEPTIBILITY TO
BERYLLIUM DISEASE, CHRONIC, SUSCEPTIBILITY TO 		0.700 0
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: 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: 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: 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: 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
dbSNP: rs1042190
rs1042190 		1.000 0.080 6 33069222 missense variant T/C snv 0.24 0.28
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
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: rs1126542
rs1126542 		1.000 0.080 6 33069647 missense variant T/A;C;G snv 0.24 0.28
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs1126769
rs1126769 		1.000 0.080 6 33068658 missense variant T/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: 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: rs12722013
rs12722013 		6 33080683 missense variant T/C;G snv 6.2E-02; 4.1E-06
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		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
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
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: 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: 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