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: rs10195252
rs10195252
0.925 0.080 2 164656581 intron variant T/C snv 0.48
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2010 2010
dbSNP: rs13389219
rs13389219
1.000 0.080 2 164672366 intron variant C/T snv 0.47
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012