Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs972936
IGF1 ; LINC02456
0.807 0.200 12 102431143 intron variant T/C snv 0.70 12
rs5742612
LOC105369944 ; IGF1
0.752 0.440 12 102481086 intron variant A/G snv 5.6E-02 11
rs1520220
LINC02456 ; IGF1
0.807 0.280 12 102402744 intron variant G/C;T snv 0.76 9
rs7136446
IGF1 ; LINC02456
0.882 0.160 12 102444737 intron variant C/T snv 0.66 8
rs2162679
IGF1
0.851 0.240 12 102477481 intron variant C/G;T snv 6
rs12423791
IGF1
0.925 0.040 12 102465050 intron variant G/C snv 2.8E-02 5
rs5742632
LINC02456 ; IGF1
0.851 0.120 12 102462696 intron variant A/G snv 0.26 4
rs5742626
LINC02456 ; IGF1
12 102464131 intron variant T/C snv 2.3E-02 3
rs2072592
IGF1 ; LINC02456
0.925 0.120 12 102419854 intron variant C/T snv 2.8E-02 2
rs2288377
LOC105369944 ; IGF1
0.925 0.080 12 102480984 intron variant A/G;T snv 2
rs4764887
IGF1 ; LINC02456
0.925 0.080 12 102430122 intron variant G/A snv 2.2E-02 2
rs5742692
LINC02456 ; IGF1
12 102405820 intron variant A/G snv 6.6E-02 2
rs7956547
IGF1
0.925 0.120 12 102465038 intron variant T/C snv 0.25 2
rs978458
IGF1 ; LINC02456
0.925 0.120 12 102408461 intron variant T/C snv 0.69 2
rs5742617
IGF1
12 102476127 intron variant C/T snv 8.7E-03 1
rs5742643
LINC02456 ; IGF1
12 102444085 intron variant T/C snv 0.76 1
rs5742663
IGF1 ; LINC02456
12 102430212 intron variant T/A;G snv 1
rs5742683
LINC02456 ; IGF1
12 102419939 intron variant A/G snv 3.3E-02 1
rs7300373
IGF1 ; LINC02456
12 102438008 intron variant T/G snv 1.4E-02 1
rs9308315
LINC02456 ; IGF1
12 102410115 intron variant A/C;T snv 1
rs1239905891
IGF1
0.925 0.080 12 102475786 missense variant G/A;T snv 3
rs745410279
IGF1
0.925 0.200 12 102478498 missense variant T/C snv 4.1E-06 2
rs121912430
LINC02456 ; IGF1
1.000 0.120 12 102419637 missense variant C/T snv 1
rs587779350
LINC02456 ; IGF1
1.000 0.120 12 102419619 missense variant G/A snv 7.0E-06 1
rs748799635
IGF1
1.000 0.080 12 102475727 missense variant C/T snv 8.0E-06 1