Source: GWASDB

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 1 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 1 2009 2019
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: 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: C0523744
Disease: Lipids measurement
Lipids measurement
0.800 1.000 1 2012 2016
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2010 2013
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2009 2009
dbSNP: rs174547
rs174547
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011