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: 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: 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: rs711752
rs711752
CETP
10 1.000 0.040 16 56962299 splice region variant G/A;C snv 0.700 1.000 3 2008 2013
dbSNP: rs10750097
rs10750097
APOA5
6 1.000 0.040 11 116793324 upstream gene variant G/A;C snv 0.700 1.000 2 2012 2012
dbSNP: rs12686004
rs12686004
ABCA1
6 1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 0.700 1.000 2 2011 2012
dbSNP: rs17482753
rs17482753 		8 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 0.700 1.000 2 2008 2012
dbSNP: rs2271293
rs2271293
NUTF2
3 1.000 0.040 16 67868167 intron variant G/A snv 0.11 0.700 1.000 2 2009 2009
dbSNP: rs2338104
rs2338104
KCTD10
3 1.000 0.040 12 109457363 non coding transcript exon variant C/G snv 0.58 0.700 1.000 2 2008 2009
dbSNP: rs2925979
rs2925979
CMIP
10 1.000 0.080 16 81501185 intron variant T/A;C snv 0.700 1.000 2 2010 2013
dbSNP: rs4810479
rs4810479 		7 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 0.700 1.000 2 2012 2012
dbSNP: rs4939883
rs4939883
LOC105372112
5 1.000 0.040 18 49640844 TF binding site variant T/C;G snv 0.700 1.000 2 2009 2009
dbSNP: rs5883
rs5883
CETP
5 1.000 0.040 16 56973441 synonymous variant C/T snv 5.1E-02 6.6E-02 0.700 1.000 2 2012 2012
dbSNP: rs7134594
rs7134594
MMAB
4 1.000 0.200 12 109562388 intron variant C/G;T snv 0.700 1.000 2 2010 2013
dbSNP: rs9987289
rs9987289
LOC157273
10 1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 0.700 1.000 2 2010 2013
dbSNP: rs10096633
rs10096633 		8 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs1059507
rs1059507
LPL
4 1.000 0.080 8 19966452 3 prime UTR variant C/T snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs11216126
rs11216126 		4 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs11570255
rs11570255
EDN3
7 1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 0.700 1.000 1 2012 2012
dbSNP: rs11820589
rs11820589
BUD13
5 1.000 0.040 11 116763146 missense variant G/A snv 7.8E-02 0.10 0.700 1.000 1 2012 2012
dbSNP: rs11986942
rs11986942 		5 1.000 0.040 8 20009934 intergenic variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs12286037
rs12286037
ZPR1
6 1.000 0.040 11 116781491 intron variant C/T snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs12447924
rs12447924
CETP
3 1.000 16 56960280 upstream gene variant C/T snv 0.76 0.700 1.000 1 2012 2012
dbSNP: rs12449157
rs12449157
GFOD2
4 1.000 0.040 16 67674994 3 prime UTR variant A/G snv 0.30 0.700 1.000 1 2010 2010
dbSNP: rs12597002
rs12597002
CETP
3 1.000 16 56968492 intron variant C/A snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs12748152
rs12748152 		8 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 0.700 1.000 1 2013 2013