rs7016880, None

N. diseases: 2
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.
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 8 20019235 intergenic variant G/C snv 8.5E-02 0.800 1.000 1 2010 2010
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 8 20019235 intergenic variant G/C snv 8.5E-02 0.700 1.000 1 2012 2012