Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6214
LINC02456 ; HELLPAR ; IGF1
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs35767
IGF1 ; LOC105369944
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs1520220
LINC02456 ; IGF1
0.807 0.280 12 102402744 intron variant G/C;T snv 0.76 9
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
rs12423791
IGF1
0.925 0.040 12 102465050 intron variant G/C snv 2.8E-02 5
rs6220
LINC02456 ; HELLPAR ; IGF1
0.925 0.080 12 102400737 3 prime UTR variant G/A snv 0.67 4