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: 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: 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: rs2066992
rs2066992
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
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
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
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
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
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
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
0.851 0.200 7 22727814 intron variant A/G;T snv
Systemic Inflammatory Response Syndrome
0.010 1.000 1 2012 2012
dbSNP: rs2069832
rs2069832
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
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: rs1524107
rs1524107
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
0.827 0.320 7 22728600 non coding transcript exon variant C/T snv 9.4E-02
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2016 2016
dbSNP: rs1524107
rs1524107
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
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
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
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: rs2069840
rs2069840
0.742 0.360 7 22728953 intron variant C/G snv 0.27
CUI: C0221775
Disease: Lumbar disc disease
Lumbar disc disease
0.010 1.000 1 2017 2017
dbSNP: rs2069840
rs2069840
0.742 0.360 7 22728953 intron variant C/G snv 0.27
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2019 2019