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: rs55791371
rs55791371
SMARCA4
3 0.925 0.080 19 11077477 intron variant A/C snv 0.11 0.800 1.000 1 2012 2012
dbSNP: rs10889353
rs10889353
DOCK7
5 1 62652525 intron variant A/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs12713956
rs12713956
APOB
4 2 21018633 intron variant A/G snv 0.14 0.700 1.000 1 2013 2013
dbSNP: rs312985
rs312985 		2 2 21155933 regulatory region variant A/G snv 0.75 0.700 1.000 1 2009 2009
dbSNP: rs4803750
rs4803750
BCL3
22 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 0.700 1.000 1 2009 2009
dbSNP: rs7228085
rs7228085
LOC105372112
1 18 49634444 intergenic variant A/G snv 0.53 0.800 1.000 1 2012 2012
dbSNP: rs1532085
rs1532085
ALDH1A2
13 0.882 0.080 15 58391167 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs11075253
rs11075253
PDXDC1 ; NTAN1
1 16 15054789 intron variant C/A snv 0.22 0.800 1.000 1 2012 2012
dbSNP: rs1167998
rs1167998
DOCK7
6 1 62465961 intron variant C/A snv 0.57 0.700 1.000 1 2009 2009
dbSNP: rs1532624
rs1532624
CETP
12 0.851 0.160 16 56971567 intron variant C/A snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs3764261
rs3764261 		26 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 0.800 1.000 1 2012 2012
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 1 2009 2009
dbSNP: rs4245791
rs4245791
ABCG8
8 0.882 0.080 2 43847292 non coding transcript exon variant C/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs181807530
rs181807530
MINK1
1 17 4871519 intron variant C/G snv 4.8E-03 0.700 1.000 1 2016 2016
dbSNP: rs17610395
rs17610395
CPT1A
1 11 68794860 missense variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2229738
rs2229738
CPT1A
2 11 68794860 missense variant C/G;T snv 6.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs7499892
rs7499892
CETP
7 16 56972678 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1160985
rs1160985
TOMM40
6 1.000 0.080 19 44900155 intron variant C/T snv 0.52 0.700 1.000 1 2013 2013
dbSNP: rs13247874
rs13247874
MLXIPL
1 7 73596112 intron variant C/T snv 0.15 0.15 0.800 1.000 1 2012 2012
dbSNP: rs17111684
rs17111684
USP24
4 1 55159875 intron variant C/T snv 3.8E-02 0.700 1.000 1 2013 2013
dbSNP: rs17249141
rs17249141
LDLR
4 19 11089332 upstream gene variant C/T snv 3.3E-03 0.700 1.000 1 2013 2013
dbSNP: rs646776
rs646776
CELSR2
25 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.700 1.000 1 2009 2009
dbSNP: rs651821
rs651821
APOA5
17 0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 0.800 1.000 1 2012 2012
dbSNP: rs72669744
rs72669744 		1 1 55650832 intron variant C/T snv 2.8E-02 0.800 1.000 1 2012 2012
dbSNP: rs7412
rs7412
APOE
47 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.800 1.000 1 2012 2012