Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0042166
Disease: Uveitis, Intermediate
Uveitis, Intermediate 		0.010 1.000 1 2015 2015
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0042164
Disease: Uveitis
Uveitis 		0.010 1.000 1 2015 2015
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0042029
Disease: Urinary tract infection
Urinary tract infection 		0.010 1.000 1 2015 2015
dbSNP: rs777906302
rs777906302
IL6 ; IL6-AS1
0.925 0.160 7 22728782 synonymous variant A/G;T snv 4.0E-06
CUI: C0042029
Disease: Urinary tract infection
Urinary tract infection 		0.010 1.000 1 2019 2019
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		0.010 1.000 1 2016 2016
dbSNP: rs2069837
rs2069837
IL6 ; IL6-AS1
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		0.040 1.000 4 2018 2020
dbSNP: rs1800796
rs1800796
IL6 ; STEAP1B ; IL6-AS1
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		0.020 1.000 2 2012 2018
dbSNP: rs2069837
rs2069837
IL6 ; IL6-AS1
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		0.010 1.000 1 2019 2019
dbSNP: rs1524107
rs1524107
IL6 ; IL6-AS1
0.827 0.320 7 22728600 non coding transcript exon variant C/T snv 9.4E-02
CUI: C1857276
Disease: Trichohepatoenteric Syndrome
Trichohepatoenteric Syndrome 		0.010 1.000 1 2010 2010
dbSNP: rs1800797
rs1800797
IL6 ; STEAP1B ; IL6-AS1
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C1857276
Disease: Trichohepatoenteric Syndrome
Trichohepatoenteric Syndrome 		0.010 1.000 1 2017 2017
dbSNP: rs1800796
rs1800796
IL6 ; STEAP1B ; IL6-AS1
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0080233
Disease: Tooth Loss
Tooth Loss 		0.010 1.000 1 2015 2015
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0040264
Disease: Tinnitus
Tinnitus 		0.010 1.000 1 2016 2016
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		0.010 1.000 1 2015 2015
dbSNP: rs1800796
rs1800796
IL6 ; STEAP1B ; IL6-AS1
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0151945
Disease: Thrombosis of cerebral veins
Thrombosis of cerebral veins 		0.010 1.000 1 2015 2015
dbSNP: rs2069837
rs2069837
IL6 ; IL6-AS1
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0039263
Disease: Takayasu Arteritis
Takayasu Arteritis 		0.720 1.000 2 2015 2019
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0039263
Disease: Takayasu Arteritis
Takayasu Arteritis 		0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.010 1.000 1 2012 2012
dbSNP: rs2069827
rs2069827
IL6 ; STEAP1B ; IL6-AS1
1.000 0.040 7 22725837 non coding transcript exon variant G/C;T snv
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.010 1.000 1 2012 2012
dbSNP: rs2069840
rs2069840
IL6 ; IL6-AS1
0.742 0.360 7 22728953 intron variant C/G snv 0.27
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.010 1.000 1 2012 2012
dbSNP: rs2069832
rs2069832
IL6 ; IL6-AS1
0.851 0.200 7 22727814 intron variant A/G;T snv
CUI: C0242966
Disease: Systemic Inflammatory Response Syndrome
Systemic Inflammatory Response Syndrome 		0.010 1.000 1 2012 2012
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0038354
Disease: Stomach Diseases
Stomach Diseases 		0.010 1.000 1 2019 2019
dbSNP: rs1800796
rs1800796
IL6 ; STEAP1B ; IL6-AS1
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0038354
Disease: Stomach Diseases
Stomach Diseases 		0.010 1.000 1 2019 2019
dbSNP: rs1800797
rs1800797
IL6 ; STEAP1B ; IL6-AS1
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C0038354
Disease: Stomach Diseases
Stomach Diseases 		0.010 1.000 1 2019 2019
dbSNP: rs1800796
rs1800796
IL6 ; STEAP1B ; IL6-AS1
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.040 1.000 4 2012 2019