rs3822072, FAM13A

N. diseases: 5
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 4 88820118 intron variant G/A;C snv 0.800 1.000 3 2013 2018
Body mass index procedure
CUI: C0005893
Disease: Body mass index procedure
252 4 88820118 intron variant G/A;C snv 0.700 1.000 1 2012 2012
Finding of body mass index
CUI: C0578022
Disease: Finding of body mass index
252 4 88820118 intron variant G/A;C snv 0.700 1.000 1 2012 2012
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 4 88820118 intron variant G/A;C snv 0.700 1.000 1 2013 2013
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 4 88820118 intron variant G/A;C snv 0.700 1.000 1 2018 2018