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: 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: rs1131690781
rs1131690781
1.000 0.040 21 31668550 missense variant C/A;G snv
CUI: C0085084
Disease: Motor Neuron Disease
Motor Neuron Disease
0.700 1.000 1 2017 2017
dbSNP: rs11556620
rs11556620
1.000 0.080 21 31667278 missense variant A/G;T snv
CUI: C1862939
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
AMYOTROPHIC LATERAL SCLEROSIS 1
0.800 1.000 3 2005 2012
dbSNP: rs1169198442
rs1169198442
1.000 0.080 21 31659837 missense variant A/G;T snv
CUI: C1862939
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
AMYOTROPHIC LATERAL SCLEROSIS 1
0.700 1.000 20 1993 2009
dbSNP: rs1202989817
rs1202989817
0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.020 1.000 2 2006 2012
dbSNP: rs1202989817
rs1202989817
0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06
CUI: C0004096
Disease: Asthma
Asthma
0.020 0.500 2 2004 2011
dbSNP: rs1202989817
rs1202989817
0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 1.000 1 2006 2006
dbSNP: rs1202989817
rs1202989817
0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2007 2007
dbSNP: rs1202989817
rs1202989817
0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome
0.010 1.000 1 2011 2011
dbSNP: rs1202989817
rs1202989817
0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06
CUI: C0004763
Disease: Barrett Esophagus
Barrett Esophagus
0.010 1.000 1 2010 2010
dbSNP: rs1202989817
rs1202989817
0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2008 2008