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: 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: 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: rs777906302
rs777906302
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
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
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: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.040 1.000 4 2011 2017
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.040 1.000 4 2012 2019
dbSNP: rs1800796
rs1800796
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
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
Diabetes Mellitus, Non-Insulin-Dependent
0.040 1.000 4 2006 2017
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.040 1.000 4 2010 2019
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.030 0.667 3 2014 2018
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.030 1.000 3 2007 2018
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.030 1.000 3 2007 2018
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.030 0.667 3 2014 2018
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.030 0.667 3 2014 2018
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.020 1.000 2 2009 2009
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.020 1.000 2 2007 2017
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.020 1.000 2 2007 2017
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.020 1.000 2 2015 2016
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0028754
Disease: Obesity
Obesity
0.020 1.000 2 2014 2019
dbSNP: rs1800796
rs1800796
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: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.020 1.000 2 2015 2016