Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 15
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 14
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38 13
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 12
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 12
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 11
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 10
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 10
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 10