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: 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: rs1474348
rs1474348
IL6 ; IL6-AS1
0.882 0.080 7 22728289 intron variant C/G snv 0.71
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs1474348
rs1474348
IL6 ; IL6-AS1
0.882 0.080 7 22728289 intron variant C/G snv 0.71
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs1474348
rs1474348
IL6 ; IL6-AS1
0.882 0.080 7 22728289 intron variant C/G snv 0.71
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.010 1.000 1 2017 2017
dbSNP: rs1474348
rs1474348
IL6 ; IL6-AS1
0.882 0.080 7 22728289 intron variant C/G snv 0.71
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.010 1.000 1 2017 2017
dbSNP: rs1524107
rs1524107
IL6 ; IL6-AS1
0.827 0.320 7 22728600 non coding transcript exon variant C/T snv 9.4E-02
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium 		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: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2016 2016
dbSNP: rs1524107
rs1524107
IL6 ; IL6-AS1
0.827 0.320 7 22728600 non coding transcript exon variant C/T snv 9.4E-02
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		0.010 1.000 1 2016 2016
dbSNP: rs1524107
rs1524107
IL6 ; IL6-AS1
0.827 0.320 7 22728600 non coding transcript exon variant C/T snv 9.4E-02
CUI: C0221775
Disease: Lumbar disc disease
Lumbar disc disease 		0.010 1.000 1 2017 2017
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: rs1524107
rs1524107
IL6 ; IL6-AS1
0.827 0.320 7 22728600 non coding transcript exon variant C/T snv 9.4E-02
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs1554606
rs1554606
IL6 ; IL6-AS1
0.925 0.120 7 22729088 intron variant T/A;G snv
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		0.010 < 0.001 1 2019 2019
dbSNP: rs1554606
rs1554606
IL6 ; IL6-AS1
0.925 0.120 7 22729088 intron variant T/A;G snv
CUI: C0028754
Disease: Obesity
Obesity 		0.010 1.000 1 2014 2014
dbSNP: rs2066992
rs2066992
IL6 ; IL6-AS1
0.807 0.200 7 22728630 non coding transcript exon variant G/T snv 9.4E-02
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		0.010 1.000 1 2014 2014
dbSNP: rs2066992
rs2066992
IL6 ; IL6-AS1
0.807 0.200 7 22728630 non coding transcript exon variant G/T snv 9.4E-02
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium 		0.010 1.000 1 2019 2019
dbSNP: rs2066992
rs2066992
IL6 ; IL6-AS1
0.807 0.200 7 22728630 non coding transcript exon variant G/T snv 9.4E-02
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.010 1.000 1 2017 2017
dbSNP: rs2066992
rs2066992
IL6 ; IL6-AS1
0.807 0.200 7 22728630 non coding transcript exon variant G/T snv 9.4E-02
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs2066992
rs2066992
IL6 ; IL6-AS1
0.807 0.200 7 22728630 non coding transcript exon variant G/T snv 9.4E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2015 2015
dbSNP: rs2066992
rs2066992
IL6 ; IL6-AS1
0.807 0.200 7 22728630 non coding transcript exon variant G/T snv 9.4E-02
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs2069832
rs2069832
IL6 ; IL6-AS1
0.851 0.200 7 22727814 intron variant A/G;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2008 2008
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: rs2069832
rs2069832
IL6 ; IL6-AS1
0.851 0.200 7 22727814 intron variant A/G;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2008 2008
dbSNP: rs2069832
rs2069832
IL6 ; IL6-AS1
0.851 0.200 7 22727814 intron variant A/G;T snv
CUI: C0004096
Disease: Asthma
Asthma 		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: C0023529
Disease: Leukomalacia, Periventricular
Leukomalacia, Periventricular 		0.010 1.000 1 2014 2014
dbSNP: rs2069837
rs2069837
IL6 ; IL6-AS1
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		0.010 1.000 1 2014 2014