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: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.700 1.000 1 2016 2016
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2016 2016
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0428302
Disease: Calcium level result
Calcium level result
0.700 1.000 1 2013 2013
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement
0.700 1.000 1 2010 2010
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C1261430
Disease: Fasting blood sugar result
Fasting blood sugar result
0.700 1.000 1 2012 2012
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2014 2014
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
High density lipoprotein measurement
0.700 1.000 1 2016 2016
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0919677
Disease: Protein C measurement
Protein C measurement
0.700 1.000 1 2010 2010
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2008 2008
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0017741
Disease: Glucose tolerance test
Glucose tolerance test
0.700 1.000 1 2018 2018
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index
0.700 1.000 1 2012 2012
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.710 1.000 2 2010 2016
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.730 1.000 4 2010 2017
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0011847
Disease: Diabetes
Diabetes
0.740 1.000 5 2010 2016
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.740 1.000 5 2010 2016
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease
0.790 1.000 10 2011 2019
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 10 2007 2019
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement
0.800 1.000 7 2010 2019
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.800 1.000 4 2010 2017
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2012 2019