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: rs28730839
rs28730839
ACE
17 63483140 missense variant C/A;G snv 4.0E-06; 4.8E-04
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs28730839
rs28730839
ACE
17 63483140 missense variant C/A;G snv 4.0E-06; 4.8E-04
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4329
rs4329
ACE
17 63486097 intron variant A/C;G snv
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		0.700 1.000 1 2011 2011
dbSNP: rs4329
rs4329
ACE
17 63486097 intron variant A/C;G snv
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		0.700 1.000 1 2011 2011
dbSNP: rs4343
rs4343
ACE
0.742 0.480 17 63488670 synonymous variant G/A snv 0.53
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2014 2014
dbSNP: rs4351
rs4351
ACE
0.925 0.160 17 63492371 intron variant G/A snv 0.50
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013