rs7205804, CETP

N. diseases: 6
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 16 56970977 intron variant G/A snv 0.34 0.800 1.000 3 2008 2019
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 16 56970977 intron variant G/A snv 0.34 0.800 1.000 2 2009 2018
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 16 56970977 intron variant G/A snv 0.34 0.700 1.000 1 2018 2018
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 16 56970977 intron variant G/A snv 0.34 0.700 1.000 1 2012 2012
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 16 56970977 intron variant G/A snv 0.34 0.700 1.000 1 2008 2008
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 16 56970977 intron variant G/A snv 0.34 0.700 1.000 1 2018 2018