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: 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: rs2069825
rs2069825
1.000 0.040 7 22725718 non coding transcript exon variant -/CC delins 6.7E-05
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.010 1.000 1 2011 2011
dbSNP: rs2069825
rs2069825
1.000 0.040 7 22725718 non coding transcript exon variant -/CC delins 6.7E-05
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
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: 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: 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: 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