rs4129767, PGS1

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
1440 17 78407903 intron variant G/A snv 0.46 0.800 1.000 4 2010 2019
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 17 78407903 intron variant G/A snv 0.46 0.700 1.000 2 2010 2013
Corpuscular Hemoglobin Concentration Mean
4389 17 78407903 intron variant G/A snv 0.46 0.700 1.000 1 2012 2012
Low density lipoprotein cholesterol measurement
1142 17 78407903 intron variant G/A snv 0.46 0.700 1.000 1 2018 2018
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 17 78407903 intron variant G/A snv 0.46 0.700 1.000 1 2018 2018
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 17 78407903 intron variant G/A snv 0.46 0.700 1.000 1 2018 2018