rs12679834, LPL

N. diseases: 7
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.
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 8 19962922 intron variant T/C snv 9.4E-02 0.700 1.000 2 2012 2012
High density lipoprotein measurement
1440 8 19962922 intron variant T/C snv 9.4E-02 0.700 1.000 1 2012 2012
Pseudocholinesterase Measurement
CUI: C1168443
Disease: Pseudocholinesterase Measurement
568 8 19962922 intron variant T/C snv 9.4E-02 0.700 1.000 1 2011 2011
RDW - Red blood cell distribution width result
988 8 19962922 intron variant T/C snv 9.4E-02 0.700 1.000 1 2019 2019
Red cell distribution width determination
988 8 19962922 intron variant T/C snv 9.4E-02 0.700 1.000 1 2019 2019
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 8 19962922 intron variant T/C snv 9.4E-02 0.700 1.000 1 2012 2012
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 8 19962922 intron variant T/C snv 9.4E-02 0.700 1.000 1 2012 2012