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: rs12158587
rs12158587
22 25623573 intron variant A/C snv 2.8E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs1351452
rs1351452
11 117072638 intron variant A/C snv 0.86
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2009 2009
dbSNP: rs16991720
rs16991720
21 34484464 intron variant A/C snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs2227368
rs2227368
19 16896136 non coding transcript exon variant A/C snv 6.6E-03 2.6E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs34515106
rs34515106
2 68380846 missense variant A/C snv 6.7E-03 1.9E-03
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs3827216
rs3827216
APP
21 25924954 intron variant A/C snv 1.7E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs453789
rs453789
17 44118647 intron variant A/C snv 0.97
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs480392
rs480392
1 107436774 synonymous variant A/C snv 0.99 0.95
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs6726798
rs6726798
2 218436132 intron variant A/C snv 0.94
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs6872314
rs6872314
5 75440240 intron variant A/C snv 0.35
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2009 2009
dbSNP: rs6951033
rs6951033
7 142636699 upstream gene variant A/C snv 0.12
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs7000460
rs7000460
LPL
8 19946291 intron variant A/C snv 7.9E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs7203984
rs7203984
16 56965346 intron variant A/C snv 0.31
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2009 2009
dbSNP: rs7926960
rs7926960
11 116783370 intron variant A/C snv 1.5E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs8077889
rs8077889
17 43800798 downstream gene variant A/C snv 0.19
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2013 2013
dbSNP: rs9340922
rs9340922
6 151971471 intron variant A/C snv 5.1E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs16981094
rs16981094
19 16078757 intron variant A/C;G snv 3.3E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs1975802
rs1975802
1.000 0.040 16 68251944 intron variant A/C;G snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2009 2009
dbSNP: rs2075847
rs2075847
11 102799093 intron variant A/C;G snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs2980875
rs2980875
8 125469505 intron variant A/C;G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2012 2019
dbSNP: rs10789117
rs10789117
1 62606594 intron variant A/C;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs10889353
rs10889353
1 62652525 intron variant A/C;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2009 2019
dbSNP: rs13022873
rs13022873
0.882 0.120 2 27592643 intron variant A/C;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2011 2011
dbSNP: rs485671
rs485671
15 58448935 intron variant A/C;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs486394
rs486394
1.000 0.040 11 116655605 intron variant A/C;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012