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: rs328
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 6 2007 2019
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 5 2007 2019
dbSNP: rs1800775
rs1800775
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2007 2009
dbSNP: rs4420638
rs4420638
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2007 2018
dbSNP: rs693
rs693
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2007 2019
dbSNP: rs17482753
rs17482753
1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2007 2019
dbSNP: rs1260326
rs1260326
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 7 2008 2019
dbSNP: rs17145738
rs17145738
0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 5 2008 2019
dbSNP: rs4846914
rs4846914
0.925 0.080 1 230159944 intron variant G/A snv 0.45
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 4 2008 2019
dbSNP: rs10503669
rs10503669
0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 3 2008 2019
dbSNP: rs16996148
rs16996148
0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 3 2008 2012
dbSNP: rs17321515
rs17321515
0.776 0.200 8 125474167 intron variant A/G snv 0.49
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 3 2008 2019
dbSNP: rs174546
rs174546
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 3 2008 2019
dbSNP: rs28927680
rs28927680
11 116748357 3 prime UTR variant C/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 3 2008 2019
dbSNP: rs12130333
rs12130333
1.000 0.080 1 62726106 regulatory region variant C/T snv 0.16
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2008 2019
dbSNP: rs12286037
rs12286037
1.000 0.040 11 116781491 intron variant C/T snv 0.11
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2008 2019
dbSNP: rs1558861
rs1558861
11 116736721 regulatory region variant C/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2008 2019
dbSNP: rs17410914
rs17410914
8 19985951 intergenic variant C/A;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2008 2012
dbSNP: rs174576
rs174576
0.851 0.200 11 61836038 intron variant C/A;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2008 2012
dbSNP: rs1748195
rs1748195
0.851 0.120 1 62583922 intron variant C/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2008 2019
dbSNP: rs2075292
rs2075292
11 116861796 intron variant G/T snv 0.80 0.86
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2008 2019
dbSNP: rs2144300
rs2144300
0.882 0.040 1 230159169 intron variant C/T snv 0.44
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2008 2018
dbSNP: rs326
rs326
LPL
8 19961928 intron variant A/G snv 0.37
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2008 2019
dbSNP: rs4775041
rs4775041
1.000 0.040 15 58382496 intron variant G/C snv 0.24
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2008 2018
dbSNP: rs10892151
rs10892151
1.000 11 117661016 intron variant C/T snv 9.7E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2008 2008