Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4925386
LAMA5
0.776 0.080 20 62345988 intron variant T/C snv 0.56 14
rs6691170 0.776 0.080 1 221872104 intergenic variant G/T snv 0.34 12
rs11874392
SMAD7
0.763 0.080 18 48926786 intron variant A/T snv 0.50 11
rs4791171
AXIN2
0.763 0.080 17 65545379 intron variant T/C snv 0.55 11
rs11169552
ATF1
0.776 0.080 12 50761880 upstream gene variant C/T snv 0.23 10
rs2238126
ETV6
0.776 0.080 12 11856807 intron variant A/G snv 0.18 10
rs2965667 0.776 0.080 12 17291799 intergenic variant A/T snv 0.96 10
rs647161
C5orf66
0.776 0.080 5 135163402 intron variant C/A snv 0.63 10
rs2555639 0.851 0.080 4 174540379 non coding transcript exon variant T/C snv 0.38 7
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs115797771
KLF5
0.807 0.080 13 73064505 intron variant A/C snv 5.8E-02 6
rs1924966 0.807 0.080 13 72432915 intergenic variant T/G snv 0.33 6
rs314277
LIN28B
0.925 0.080 6 104959787 intron variant A/C;G;T snv 6
rs6854845 0.827 0.080 4 74821455 intergenic variant G/T snv 0.13 6
rs1057519860
EGFR
0.851 0.080 7 55160316 missense variant C/A snv 5
rs12037879
LEPR
0.925 0.080 1 65477024 intron variant G/A;T snv 5
rs1289280947
CDKN2A
0.851 0.080 9 21974571 missense variant C/T snv 4.0E-06 5
rs146639652
POLE
0.827 0.080 12 132675752 missense variant G/A;C snv 1.2E-05 5
rs9365723
SYNJ2
0.827 0.080 6 158014540 intron variant A/C;G snv 0.56 5
rs1051690
INSR
0.851 0.080 19 7116952 3 prime UTR variant T/C snv 0.83 4
rs1064795747
MSH2
0.925 0.080 2 47412433 missense variant T/C snv 4
rs1064795841
TP53
0.882 0.080 17 7674971 missense variant C/T snv 4
rs1088967 0.851 0.080 X 127010099 intergenic variant T/A;C snv 4
rs138551214
EPHB2
0.925 0.080 1 22909025 missense variant G/A snv 4.0E-06 1.4E-05 4
rs1535989 0.925 0.080 13 105370372 intergenic variant A/G;T snv 4