Source: GWASCAT

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: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 1 2011 2019
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
High density lipoprotein measurement
0.800 1.000 4 2009 2019
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 3 2009 2019
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0523744
Disease: Lipids measurement
Lipids measurement
0.800 1.000 2 2012 2016
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0337438
Disease: Glucose measurement
Glucose measurement
0.800 1.000 1 2011 2016
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level
0.800 1.000 1 2011 2016
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE
0.800 1.000 1 2010 2010
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 3 2016 2019
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.700 1.000 1 2016 2016
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.700 1.000 1 2016 2016
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.700 1.000 1 2016 2016
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2019 2019
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0011847
Disease: Diabetes
Diabetes
0.700 1.000 1 2016 2016
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2015 2015
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2016 2016
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2016 2016
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0018801
Disease: Heart failure
Heart failure
0.700 1.000 1 2016 2016