Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5742612
LOC105369944 ; IGF1
0.752 0.440 12 102481086 intron variant A/G snv 5.6E-02 11
rs4764887
IGF1 ; LINC02456
0.925 0.080 12 102430122 intron variant G/A snv 2.2E-02 2
rs35767
IGF1 ; LOC105369944
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs2288377
LOC105369944 ; IGF1
0.925 0.080 12 102480984 intron variant A/G;T snv 2
rs2195239
LINC02456 ; IGF1
0.851 0.240 12 102462924 non coding transcript exon variant C/G snv 0.28 7
rs2162679
IGF1
0.851 0.240 12 102477481 intron variant C/G;T snv 6
rs2072592
IGF1 ; LINC02456
0.925 0.120 12 102419854 intron variant C/T snv 2.8E-02 2
rs1520220
LINC02456 ; IGF1
0.807 0.280 12 102402744 intron variant G/C;T snv 0.76 9
rs12423791
IGF1
0.925 0.040 12 102465050 intron variant G/C snv 2.8E-02 5
rs1239905891
IGF1
0.925 0.080 12 102475786 missense variant G/A;T snv 3
rs121912430
LINC02456 ; IGF1
1.000 0.120 12 102419637 missense variant C/T snv 1