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: 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: 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: 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: 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: 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: rs173539
rs173539 		11 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 0.700 1.000 2 2009 2011
dbSNP: rs2083637
rs2083637 		6 0.925 0.080 8 20007664 intergenic variant A/G snv 0.25 0.700 1.000 2 2009 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: 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: rs7120118
rs7120118
NR1H3
18 0.716 0.360 11 47264739 intron variant T/C snv 0.38 0.700 1.000 2 2009 2012
dbSNP: rs157580
rs157580
TOMM40
14 0.882 0.160 19 44892009 intron variant G/A snv 0.69 0.700 1.000 1 2009 2009
dbSNP: rs174547
rs174547
FADS1 ; FADS2
33 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.700 1.000 1 2009 2009
dbSNP: rs255049
rs255049
DPEP3
3 1.000 0.040 16 67979568 intron variant T/C snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs2967605
rs2967605
RAB11B
4 0.925 0.040 19 8404854 downstream gene variant C/T snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs3905000
rs3905000
ABCA1
5 0.925 0.080 9 104894789 intron variant G/A snv 0.14 0.700 1.000 1 2009 2009
dbSNP: rs471364
rs471364
TTC39B
3 1.000 0.040 9 15289580 intron variant C/T snv 0.87 0.700 1.000 1 2009 2009
dbSNP: rs6754295
rs6754295 		6 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 0.700 1.000 1 2009 2009
dbSNP: rs7395662
rs7395662 		5 0.882 0.080 11 48497341 downstream gene variant A/G snv 0.56 0.700 1.000 1 2009 2009
dbSNP: rs7679
rs7679
PCIF1
9 0.925 0.160 20 45947863 3 prime UTR variant T/C snv 0.13 0.700 1.000 1 2009 2009
dbSNP: rs9891572
rs9891572 		3 1.000 0.040 17 2525214 intergenic variant C/T snv 0.17 0.700 1.000 1 2009 2009
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: 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: rs1042034
rs1042034
APOB
15 0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 0.700 1.000 2 2010 2012
dbSNP: rs1084651
rs1084651 		2 6 160668785 intron variant G/A snv 0.23 0.700 1.000 2 2010 2012