Source: GWASCAT

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: rs964184
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.830 1.000 2 2010 2019
dbSNP: rs1260326
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.820 0.750 1 2010 2016
dbSNP: rs4635554
rs4635554 		2 21166787 intergenic variant T/G snv 0.37
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.800 1.000 1 2010 2010
dbSNP: rs7016880
rs7016880 		8 20019235 intergenic variant G/C snv 8.5E-02
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.800 1.000 1 2010 2010
dbSNP: rs780094
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.730 1.000 1 2010 2017
dbSNP: rs17145738
rs17145738
TBL2
0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.710 1.000 1 2014 2017
dbSNP: rs10808546
rs10808546 		8 125483576 intron variant C/T snv 0.39
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.700 1.000 1 2017 2017
dbSNP: rs10911205
rs10911205
LAMC1
1 183040142 intron variant C/A snv 0.33
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.700 1.000 1 2017 2017
dbSNP: rs10911232
rs10911232
LAMC1
1 183083398 intron variant C/T snv 0.33
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.700 1.000 1 2017 2017
dbSNP: rs1558861
rs1558861 		11 116736721 regulatory region variant C/G;T snv
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.700 1.000 1 2017 2017
dbSNP: rs2001945
rs2001945 		8 125465736 upstream gene variant G/A;C;T snv
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.700 1.000 1 2017 2017
dbSNP: rs2074755
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.700 1.000 1 2017 2017
dbSNP: rs3825041
rs3825041
BUD13
11 116760991 intron variant T/A;C snv 0.89
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.700 1.000 1 2017 2017
dbSNP: rs672059
rs672059
LAMC2
1 183193404 intron variant G/A snv 0.57
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.700 1.000 1 2017 2017
dbSNP: rs6982502
rs6982502 		0.882 0.080 8 125467120 intron variant C/T snv 0.62
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.700 1.000 1 2017 2017
dbSNP: rs780093
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.700 1.000 1 2017 2017