Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17145738
TBL2
0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11 11
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 7
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801177
LPL
0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 14
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs190853081
APOE
0.925 0.080 19 44909083 missense variant G/A snv 2.0E-04 5.6E-05 3
rs199768005
APOE
0.882 0.160 19 44909057 missense variant T/A snv 4.5E-04 4.9E-04 4
rs1997947
GALNT2
1.000 0.120 1 230148017 intron variant G/A snv 0.78 2
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs201079485
ZPR1 ; APOA5
0.925 0.080 11 116790940 stop gained G/A;T snv 8.0E-05; 4.0E-06 4
rs2057482
HIF1A-AS2 ; HIF1A-AS3 ; HIF1A
0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs2071282
NOTCH4
0.925 0.200 6 32221166 missense variant G/A snv 4.7E-03 1.4E-03 3
rs2074379
ALPK1
1.000 4 112431743 missense variant G/A snv 0.62 0.65 3
rs2074388
ALPK1
1.000 4 112431241 missense variant G/A snv 0.62 0.65 3
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20