Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 7
rs972283
LOC105375508
1.000 0.080 7 130782095 intergenic variant A/G;T snv 3
rs1028728
POSTN
0.925 0.040 13 37599679 upstream gene variant A/T snv 0.20 3
rs2293869
RP1
8 54626835 missense variant A/T snv 0.34 0.33 1
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs11773845
CAV1
0.925 0.120 7 116551247 intron variant C/A snv 0.53 4
rs10911205
LAMC1
1 183040142 intron variant C/A snv 0.33 1
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 7
rs6074
LIPC
15 58568764 synonymous variant C/A;G snv 0.19; 2.8E-05 1
rs11542041
APOE
0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs2075291
APOA5 ; ZPR1
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15
rs121918393
APOE
0.851 0.120 19 44908756 missense variant C/A;T snv 1.3E-05; 9.0E-05 6
rs4846913
GALNT2
1.000 0.120 1 230158968 intron variant C/A;T snv 4
rs1414423445
CREB3L3
19 4171402 stop gained C/A;T snv 4.0E-06; 4.0E-06 1
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs3812316
MLXIPL
0.763 0.240 7 73606007 missense variant C/G snv 0.10 9.4E-02 14
rs371282890
LPL
0.827 0.120 8 19955900 missense variant C/G snv 1.1E-04 6.3E-05 6
rs11202592
KLLN ; PTEN
0.851 0.200 10 87864461 5 prime UTR variant C/G snv 3.8E-03 1.4E-03 5
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16