Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs415799
rs415799
15 58398555 intron variant G/A snv 0.38
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2011 2011
dbSNP: rs415799
rs415799
15 58398555 intron variant G/A snv 0.38
High density lipoprotein measurement
0.700 1.000 1 2011 2011
dbSNP: rs415799
rs415799
15 58398555 intron variant G/A snv 0.38
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs415799
rs415799
15 58398555 intron variant G/A snv 0.38
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2009 2009