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: rs13306435
rs13306435
IL6
1.000 0.080 7 22731420 missense variant T/A;C snv 2.9E-02; 4.2E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs13306436
rs13306436
IL6
7 22731677 3 prime UTR variant G/A snv 7.2E-04
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs13306436
rs13306436
IL6
7 22731677 3 prime UTR variant G/A snv 7.2E-04
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs13306436
rs13306436
IL6
7 22731677 3 prime UTR variant G/A snv 7.2E-04
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs2069843
rs2069843
IL6
1.000 0.040 7 22730375 intron variant G/A snv 5.6E-02
CUI: C0017677
Disease: Glossitis, Benign Migratory
Glossitis, Benign Migratory
0.010 1.000 1 2017 2017
dbSNP: rs2069845
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.010 1.000 1 2017 2017
dbSNP: rs2069845
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.010 1.000 1 2018 2018
dbSNP: rs2069845
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2019 2019
dbSNP: rs2069845
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs2069845
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia
0.010 1.000 1 2019 2019
dbSNP: rs2069845
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs2069845
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61
CUI: C0004936
Disease: Mental disorders
Mental disorders
0.010 1.000 1 2018 2018
dbSNP: rs2069845
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.010 1.000 1 2017 2017
dbSNP: rs2069849
rs2069849
IL6
0.882 0.120 7 22731537 missense variant C/G;T snv 4.4E-02
CUI: C0028754
Disease: Obesity
Obesity
0.010 1.000 1 2019 2019
dbSNP: rs2069849
rs2069849
IL6
0.882 0.120 7 22731537 missense variant C/G;T snv 4.4E-02
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.010 1.000 1 2019 2019
dbSNP: rs2069849
rs2069849
IL6
0.882 0.120 7 22731537 missense variant C/G;T snv 4.4E-02
Selective immunoglobulin A deficiency
0.010 1.000 1 2008 2008
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: rs369953112
rs369953112
IL6
1.000 0.040 7 22731416 missense variant T/C snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.010 1.000 1 2011 2011
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.020 1.000 2 2013 2016
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.020 1.000 2 2013 2016
dbSNP: rs2069837
rs2069837
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: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0023980
Disease: Longevity
Longevity
0.700 1.000 2 2016 2019
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.020 1.000 2 2013 2016
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0028754
Disease: Obesity
Obesity
0.020 0.500 2 2009 2012