Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs768963
CACTIN
0.925 0.120 19 3615409 non coding transcript exon variant G/A;C snv 2
rs3731245
CDKN2A
0.925 0.120 9 21972446 intron variant C/T snv 6.6E-03 2
rs7956547
IGF1
0.925 0.120 12 102465038 intron variant T/C snv 0.25 2
rs2072592
IGF1 ; LINC02456
0.925 0.120 12 102419854 intron variant C/T snv 2.8E-02 2
rs978458
IGF1 ; LINC02456
0.925 0.120 12 102408461 intron variant T/C snv 0.69 2
rs710968
LIMK1
0.925 0.120 7 74083398 intron variant A/G snv 0.75 2
rs4245191
NLRX1
0.925 0.200 11 119182117 missense variant C/A snv 0.56 0.57 2
rs10898909
P2RY2
0.925 0.120 11 73241451 non coding transcript exon variant G/A snv 0.21 2
rs3769048
RAMP1
0.925 0.120 2 237861218 intron variant G/A snv 2.2E-02 2
rs750272074
ROS1
1.000 0.120 6 117362705 synonymous variant A/G snv 4.0E-06 2
rs2278986
SCARB1
0.925 0.120 12 124814823 intron variant A/G snv 0.28 2
rs12659
SLC19A1
0.925 0.120 21 45531642 synonymous variant A/G snv 0.58 0.57 2
rs10304
SMTN ; SELENOM
0.925 0.120 22 31104550 3 prime UTR variant G/A snv 0.12 2
rs2238634
TBXA2R
0.925 0.200 19 3604731 intron variant A/C;T snv 2
rs7590387 0.882 0.120 2 237913557 downstream gene variant G/A;C snv 3
rs3789683
F3
0.925 0.200 1 94530506 missense variant C/T snv 6.5E-03 1.0E-02 3
rs1801273
FABP1
0.925 0.200 2 88126256 missense variant C/T snv 1.2E-05 2.1E-05 3
rs2232582
LBP
0.882 0.160 20 38350862 synonymous variant T/C snv 0.16 0.22 3
rs755703581
PDX1
0.925 0.120 13 27920295 missense variant G/A snv 2.3E-05 7.0E-06 3
rs1131882
TBXA2R
0.882 0.200 19 3595925 missense variant G/A snv 0.22 0.15 3
rs12342
ADIPOR2
0.851 0.240 12 1787714 3 prime UTR variant C/A;T snv 4
rs4073259
ALOX5AP
0.882 0.160 13 30732134 intron variant G/A snv 0.49 4
rs1537378
CDKN2B-AS1
0.882 0.160 9 22061615 intron variant A/G snv 0.73 4
rs7291467
LGALS2
0.851 0.160 22 37576621 intron variant G/A snv 0.49 4
rs1050283
OLR1
0.882 0.160 12 10159690 3 prime UTR variant G/A snv 0.40 4