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: rs261342
rs261342
15 58438954 intron variant G/A;C;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2012 2019
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2012 2016
dbSNP: rs588136
rs588136
15 58438299 intron variant C/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2012 2017
dbSNP: rs261334
rs261334
15 58434545 intron variant G/C snv 0.73
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018