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: rs2308911
rs2308911 		1.000 0.080 6 33069803 missense variant T/G snv 0.23 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: 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: 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: 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
dbSNP: rs3830066
rs3830066 		1.000 0.080 6 33069410 non coding transcript exon variant C/A;G snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
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
dbSNP: rs6914995
rs6914995 		1.000 0.080 6 33072967 intron variant G/C snv 0.29
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs7751953
rs7751953 		1.000 0.080 6 33065574 non coding transcript exon 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: rs7770370
rs7770370 		0.925 0.160 6 33081144 non coding transcript exon variant A/G snv 0.27
CUI: C4048328
Disease: cervical cancer
cervical cancer 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.700 1.000 1 2013 2013
dbSNP: rs9277341
rs9277341 		0.882 0.280 6 33071848 intron variant T/A;C snv
CUI: C3495801
Disease: Granulomatosis with polyangiitis
Granulomatosis with polyangiitis 		Respiratory Tract Diseases; Immune System Diseases; Cardiovascular Diseases 0.700 1.000 1 2013 2013
dbSNP: rs9277341
rs9277341 		0.882 0.280 6 33071848 intron variant T/A;C snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2009 2009
dbSNP: rs9277341
rs9277341 		0.882 0.280 6 33071848 intron variant T/A;C snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2009 2009
dbSNP: rs9277357
rs9277357 		1.000 0.080 6 33082202 intron variant A/G snv 0.38
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs9277359
rs9277359 		0.925 0.200 6 33082247 intron variant C/A;T snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs9277359
rs9277359 		0.925 0.200 6 33082247 intron variant C/A;T snv
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: rs9277377
rs9277377 		1.000 0.120 6 33082426 intron variant C/A;G snv
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: rs9277378
rs9277378 		0.827 0.320 6 33082502 intron variant A/G snv 0.40
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2011 2011