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: rs17884057
rs17884057
0.925 0.080 21 31664502 intron variant AGA/- delins 0.13
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.020 1.000 2 2011 2013
dbSNP: rs17884057
rs17884057
0.925 0.080 21 31664502 intron variant AGA/- delins 0.13
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.020 1.000 2 2011 2013
dbSNP: rs1041740
rs1041740
0.807 0.320 21 31667849 intron variant C/T snv 0.24
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 1.000 1 2012 2012
dbSNP: rs1041740
rs1041740
0.807 0.320 21 31667849 intron variant C/T snv 0.24
Diabetes Mellitus, Insulin-Dependent
0.010 1.000 1 2018 2018
dbSNP: rs1041740
rs1041740
0.807 0.320 21 31667849 intron variant C/T snv 0.24
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.010 1.000 1 2012 2012
dbSNP: rs1041740
rs1041740
0.807 0.320 21 31667849 intron variant C/T snv 0.24
CUI: C0275551
Disease: Primary bacterial peritonitis
Primary bacterial peritonitis
0.010 1.000 1 2017 2017
dbSNP: rs1041740
rs1041740
0.807 0.320 21 31667849 intron variant C/T snv 0.24
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
0.010 1.000 1 2017 2017
dbSNP: rs1041740
rs1041740
0.807 0.320 21 31667849 intron variant C/T snv 0.24
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases
0.010 1.000 1 2011 2011
dbSNP: rs1041740
rs1041740
0.807 0.320 21 31667849 intron variant C/T snv 0.24
CUI: C0740447
Disease: Diabetic peripheral neuropathy
Diabetic peripheral neuropathy
0.010 1.000 1 2018 2018
dbSNP: rs1041740
rs1041740
0.807 0.320 21 31667849 intron variant C/T snv 0.24
CUI: C1623038
Disease: Cirrhosis
Cirrhosis
0.010 < 0.001 1 2017 2017
dbSNP: rs10432782
rs10432782
0.807 0.160 21 31664078 intron variant T/G snv 0.19
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs10432782
rs10432782
0.807 0.160 21 31664078 intron variant T/G snv 0.19
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.010 1.000 1 2012 2012
dbSNP: rs10432782
rs10432782
0.807 0.160 21 31664078 intron variant T/G snv 0.19
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 1.000 1 2012 2012
dbSNP: rs10432782
rs10432782
0.807 0.160 21 31664078 intron variant T/G snv 0.19
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2011 2011
dbSNP: rs10432782
rs10432782
0.807 0.160 21 31664078 intron variant T/G snv 0.19
CUI: C3146264
Disease: Stage IV Prostate Cancer AJCC v7
Stage IV Prostate Cancer AJCC v7
0.010 1.000 1 2015 2015
dbSNP: rs10432782
rs10432782
0.807 0.160 21 31664078 intron variant T/G snv 0.19
CUI: C0278837
Disease: Stage IV Prostate Carcinoma
Stage IV Prostate Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs10432782
rs10432782
0.807 0.160 21 31664078 intron variant T/G snv 0.19
CUI: C4553752
Disease: Stage IV Prostate Cancer AJCC v8
Stage IV Prostate Cancer AJCC v8
0.010 1.000 1 2015 2015
dbSNP: rs2234694
rs2234694
0.882 0.240 21 31666552 intron variant A/C snv 3.6E-02 3.4E-02
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.010 1.000 1 2010 2010
dbSNP: rs2234694
rs2234694
0.882 0.240 21 31666552 intron variant A/C snv 3.6E-02 3.4E-02
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.010 1.000 1 2019 2019
dbSNP: rs2234694
rs2234694
0.882 0.240 21 31666552 intron variant A/C snv 3.6E-02 3.4E-02
Diabetes Mellitus, Insulin-Dependent
0.010 1.000 1 2010 2010
dbSNP: rs4816407
rs4816407
0.925 0.080 21 31667716 intron variant A/G snv 0.15
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs4816407
rs4816407
0.925 0.080 21 31667716 intron variant A/G snv 0.15
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2011 2011
dbSNP: rs4998557
rs4998557
0.851 0.080 21 31662579 intron variant G/A snv 0.22
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs4998557
rs4998557
0.851 0.080 21 31662579 intron variant G/A snv 0.22
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2014 2014
dbSNP: rs4998557
rs4998557
0.851 0.080 21 31662579 intron variant G/A snv 0.22
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2014 2014