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: rs747126003
rs747126003
IL6 ; IL6-AS1
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma 		0.010 < 0.001 1 2017 2017
dbSNP: rs747126003
rs747126003
IL6 ; IL6-AS1
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0036690
Disease: Septicemia
Septicemia 		0.010 1.000 1 2006 2006
dbSNP: rs747126003
rs747126003
IL6 ; IL6-AS1
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C1332986
Disease: Childhood Osteosarcoma
Childhood Osteosarcoma 		0.010 < 0.001 1 2017 2017
dbSNP: rs747126003
rs747126003
IL6 ; IL6-AS1
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0585442
Disease: Osteosarcoma of bone
Osteosarcoma of bone 		0.010 < 0.001 1 2017 2017
dbSNP: rs747126003
rs747126003
IL6 ; IL6-AS1
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C3887461
Disease: Head and Neck Carcinoma
Head and Neck Carcinoma 		0.010 1.000 1 2007 2007
dbSNP: rs747126003
rs747126003
IL6 ; IL6-AS1
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0374997
Disease: Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site 		0.010 1.000 1 2017 2017
dbSNP: rs747126003
rs747126003
IL6 ; IL6-AS1
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 1.000 1 2019 2019
dbSNP: rs747126003
rs747126003
IL6 ; IL6-AS1
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.010 < 0.001 1 2012 2012
dbSNP: rs747126003
rs747126003
IL6 ; IL6-AS1
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
Malignant Head and Neck Neoplasm 		0.010 1.000 1 2007 2007
dbSNP: rs747126003
rs747126003
IL6 ; IL6-AS1
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C1704321
Disease: Nephrotic Syndrome, Minimal Change
Nephrotic Syndrome, Minimal Change 		0.010 1.000 1 2017 2017
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: rs777906302
rs777906302
IL6 ; IL6-AS1
0.925 0.160 7 22728782 synonymous variant A/G;T snv 4.0E-06
CUI: C0262655
Disease: Recurrent urinary tract infection
Recurrent urinary tract infection 		0.010 1.000 1 2019 2019
dbSNP: rs777906302
rs777906302
IL6 ; IL6-AS1
0.925 0.160 7 22728782 synonymous variant A/G;T snv 4.0E-06
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2018 2018
dbSNP: rs1474347
rs1474347
IL6 ; IL6-AS1
1.000 0.120 7 22728505 non coding transcript exon variant C/A snv 0.69
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.010 1.000 1 2014 2014
dbSNP: rs2069861
rs2069861
IL6
0.925 0.080 7 22732035 upstream gene variant C/A;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2011 2011
dbSNP: rs2069861
rs2069861
IL6
0.925 0.080 7 22732035 upstream gene variant C/A;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2011 2011
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.070 0.714 7 2009 2019
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.070 1.000 7 2006 2018
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.070 0.714 7 2009 2019
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.060 0.833 6 2010 2019
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.060 1.000 6 2007 2017
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.060 1.000 6 2007 2017
dbSNP: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.050 1.000 5 2009 2017
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: rs1800795
rs1800795
IL6 ; STEAP1B ; IL6-AS1
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.040 1.000 4 2017 2018