Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs118204057
rs118204057
LPL
16 0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 0.010 1.000 1 2008 2008
dbSNP: rs12190287
rs12190287
TCF21
19 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 0.010 1.000 1 2014 2014
dbSNP: rs121918313
rs121918313
LRP6 ; BCL2L14
4 0.851 0.080 12 12164494 missense variant G/A snv 1.6E-05 0.010 1.000 1 2011 2011
dbSNP: rs121918393
rs121918393
APOE
6 0.851 0.120 19 44908756 missense variant C/A;T snv 1.3E-05; 9.0E-05 0.010 1.000 1 2003 2003
dbSNP: rs1232898090
rs1232898090
PPARA
40 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2003 2003
dbSNP: rs1249040838
rs1249040838
LDLR ; MIR6886
5 0.827 0.120 19 11113699 missense variant G/A snv 4.0E-06 0.010 1.000 1 2003 2003
dbSNP: rs1267969615
rs1267969615
ACE
100 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs1282382243
rs1282382243
DLEU1 ; DLEU7 ; DLEU7-AS1
8 0.807 0.120 13 50843630 missense variant G/A snv 0.010 1.000 1 2001 2001
dbSNP: rs1378942
rs1378942
CSK
16 0.790 0.240 15 74785026 intron variant C/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs1384889210
rs1384889210
APOA1 ; APOA1-AS
5 0.827 0.040 11 116836193 missense variant C/A snv 0.010 1.000 1 2015 2015
dbSNP: rs1403934301
rs1403934301
SHBG
3 0.882 0.120 17 7631317 missense variant G/A snv 0.010 1.000 1 2017 2017
dbSNP: rs1440763451
rs1440763451
PPARG
4 0.882 0.080 3 12416849 missense variant A/G snv 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs1447295
rs1447295
CASC8
29 0.658 0.400 8 127472793 intron variant A/C;T snv 0.010 1.000 1 2008 2008
dbSNP: rs1490867890
rs1490867890
MCL1 ; LOC107985203
3 0.882 0.080 1 150579475 missense variant G/A;C snv 0.010 1.000 1 2015 2015
dbSNP: rs1535045
rs1535045
CD40
12 0.742 0.360 20 46119460 intron variant C/A;G;T snv 0.010 1.000 1 2012 2012
dbSNP: rs17465637
rs17465637
MIA3
11 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 0.010 < 0.001 1 2012 2012
dbSNP: rs1764391
rs1764391
GJA4 ; SMIM12 ; LOC105378642
7 0.790 0.160 1 34795168 missense variant C/G;T snv 0.30 0.010 1.000 1 2011 2011
dbSNP: rs1799889
rs1799889
SERPINE1
31 0.649 0.600 7 101126430 upstream gene variant A/G snv 0.010 1.000 1 2018 2018
dbSNP: rs1800947
rs1800947
CRP
28 0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs1801177
rs1801177
LPL
14 0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 0.010 1.000 1 2018 2018
dbSNP: rs1862513
rs1862513
RETN
11 0.763 0.360 19 7668907 upstream gene variant C/G;T snv 0.010 < 0.001 1 2011 2011
dbSNP: rs20417
rs20417
PTGS2 ; PACERR
57 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2009 2009
dbSNP: rs2106261
rs2106261
ZFHX3
11 0.763 0.160 16 73017721 intron variant C/G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs2228145
rs2228145
IL6R
57 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.010 1.000 1 2014 2014
dbSNP: rs2229238
rs2229238
IL6R
5 0.851 0.080 1 154465420 3 prime UTR variant T/A;C snv 0.80 0.010 1.000 1 2011 2011