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: rs12721046
rs12721046
19 44917997 intron variant G/A snv 0.11
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 2 2012 2012
dbSNP: rs12721046
rs12721046
19 44917997 intron variant G/A snv 0.11
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 2 2012 2012
dbSNP: rs12721046
rs12721046
19 44917997 intron variant G/A snv 0.11
High density lipoprotein measurement
0.700 1.000 2 2012 2012
dbSNP: rs12721046
rs12721046
19 44917997 intron variant G/A snv 0.11
Low density lipoprotein cholesterol measurement
0.700 1.000 2 2012 2012
dbSNP: rs12721046
rs12721046
19 44917997 intron variant G/A snv 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs12721046
rs12721046
19 44917997 intron variant G/A snv 0.11
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2013 2013
dbSNP: rs12721046
rs12721046
19 44917997 intron variant G/A snv 0.11
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs12721046
rs12721046
19 44917997 intron variant G/A snv 0.11
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012