rs2069837, IL6-AS1;IL6

N. diseases: 18
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Takayasu Arteritis
CUI: C0039263
Disease: Takayasu Arteritis
55 0.724 0.520 7 22728408 intron variant A/C;G snv 0.720 1.000 2 2015 2019
Longevity
CUI: C0023980
Disease: Longevity
74 0.724 0.520 7 22728408 intron variant A/C;G snv 0.700 1.000 2 2016 2019
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.724 0.520 7 22728408 intron variant A/C;G snv 0.020 1.000 2 2013 2016
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.724 0.520 7 22728408 intron variant A/C;G snv 0.020 1.000 2 2013 2016
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.724 0.520 7 22728408 intron variant A/C;G snv 0.020 1.000 2 2013 2016
Cerebral Palsy
CUI: C0007789
Disease: Cerebral Palsy
69 0.724 0.520 7 22728408 intron variant A/C;G snv 0.010 1.000 1 2014 2014
Chronic Periodontitis
CUI: C0266929
Disease: Chronic Periodontitis
99 0.724 0.520 7 22728408 intron variant A/C;G snv 0.010 1.000 1 2017 2017
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.724 0.520 7 22728408 intron variant A/C;G snv 0.010 1 2019 2019
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.724 0.520 7 22728408 intron variant A/C;G snv 0.010 1.000 1 2012 2012
Leukomalacia, Periventricular
CUI: C0023529
Disease: Leukomalacia, Periventricular
10 0.724 0.520 7 22728408 intron variant A/C;G snv 0.010 1.000 1 2014 2014
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.724 0.520 7 22728408 intron variant A/C;G snv 0.010 1.000 1 2016 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.724 0.520 7 22728408 intron variant A/C;G snv 0.010 1.000 1 2016 2016
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.724 0.520 7 22728408 intron variant A/C;G snv 0.010 1.000 1 2019 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.724 0.520 7 22728408 intron variant A/C;G snv 0.010 1.000 1 2016 2016
Secondary malignant neoplasm of colon and/or rectum
CUI: C4721579
Disease: Secondary malignant neoplasm of colon and/or rectum
68 0.724 0.520 7 22728408 intron variant A/C;G snv 0.010 1.000 1 2016 2016
Spastic Quadriplegia
CUI: C0426970
Disease: Spastic Quadriplegia
7 0.724 0.520 7 22728408 intron variant A/C;G snv 0.010 1.000 1 2013 2013
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
328 0.724 0.520 7 22728408 intron variant A/C;G snv 0.010 1.000 1 2019 2019
Tuberculosis, Pulmonary
CUI: C0041327
Disease: Tuberculosis, Pulmonary
171 0.724 0.520 7 22728408 intron variant A/C;G snv 0.010 1.000 1 2018 2018