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: rs3764261
rs3764261 		26 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 0.700 1.000 8 2008 2013
dbSNP: rs1532085
rs1532085
ALDH1A2
13 0.882 0.080 15 58391167 intron variant A/G;T snv 0.700 1.000 6 2009 2013
dbSNP: rs964184
rs964184
ZPR1
47 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 6 2009 2013
dbSNP: rs9989419
rs9989419 		11 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 0.700 1.000 6 2008 2014
dbSNP: rs12678919
rs12678919 		10 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 0.700 1.000 5 2009 2013
dbSNP: rs1800775
rs1800775
CETP
18 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 0.700 1.000 5 2008 2013
dbSNP: rs1883025
rs1883025
ABCA1
13 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.700 1.000 5 2009 2013
dbSNP: rs4846914
rs4846914
GALNT2
6 0.925 0.080 1 230159944 intron variant G/A snv 0.45 0.700 1.000 5 2008 2013
dbSNP: rs10503669
rs10503669 		8 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 0.700 1.000 4 2008 2012
dbSNP: rs1532624
rs1532624
CETP
12 0.851 0.160 16 56971567 intron variant C/A snv 0.34 0.700 1.000 4 2009 2013
dbSNP: rs1800961
rs1800961
HNF4A
21 0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 0.700 1.000 4 2009 2013
dbSNP: rs2156552
rs2156552
LOC105372112
6 1.000 0.040 18 49655298 downstream gene variant A/G;T snv 0.700 1.000 4 2008 2012
dbSNP: rs2954029
rs2954029 		14 0.807 0.160 8 125478730 intron variant A/T snv 0.42 0.700 1.000 4 2010 2013
dbSNP: rs5880
rs5880
CETP
10 0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02 0.700 1.000 4 2008 2014
dbSNP: rs7499892
rs7499892
CETP
7 16 56972678 intron variant C/G;T snv 0.700 1.000 4 2011 2012
dbSNP: rs10468017
rs10468017
ALDH1A2
12 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.700 1.000 3 2009 2012
dbSNP: rs13702
rs13702
LPL
7 0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 0.700 1.000 3 2012 2012
dbSNP: rs17145738
rs17145738
TBL2
11 0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11 0.700 1.000 3 2010 2013
dbSNP: rs1864163
rs1864163
CETP
10 0.882 0.120 16 56963321 intron variant G/A snv 0.26 0.700 1.000 3 2008 2012
dbSNP: rs2070895
rs2070895
LIPC ; ALDH1A2
15 0.807 0.120 15 58431740 intron variant G/A snv 0.33 0.700 1.000 3 2012 2012
dbSNP: rs255052
rs255052
DUS2 ; DPEP2
4 0.925 0.040 16 67991092 intron variant G/A snv 0.17 0.17 0.700 1.000 3 2008 2012
dbSNP: rs3890182
rs3890182
ABCA1
5 0.925 0.120 9 104885374 intron variant G/A;T snv 0.700 1.000 3 2008 2012
dbSNP: rs4775041
rs4775041
ALDH1A2
8 1.000 0.040 15 58382496 intron variant G/C snv 0.24 0.700 1.000 3 2008 2012
dbSNP: rs4783961
rs4783961
CETP
7 0.851 0.320 16 56960982 upstream gene variant G/A snv 0.48 0.47 0.700 1.000 3 2012 2012
dbSNP: rs5882
rs5882
CETP
35 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.700 1.000 3 2008 2012