Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35755165 0.882 0.080 19 40840084 intron variant A/C;G snv 5
rs36600
MTMR3
0.827 0.080 22 29941597 intron variant T/C snv 0.78 5
rs374733251
MET
0.882 0.080 7 116740993 missense variant A/G snv 6.0E-05 7.7E-05 5
rs377444977
EGFR
0.882 0.080 7 55143443 missense variant G/A snv 5.2E-05 2.1E-05 5
rs3842
ABCB1
0.882 0.080 7 87504050 3 prime UTR variant T/C snv 0.16 5
rs4488809
TP63
0.827 0.080 3 189638472 intron variant T/C snv 0.45 5
rs4647958
SNAI1
0.851 0.080 20 49984094 missense variant T/C snv 0.18 0.29 5
rs533748068
ARHGEF2 ; MIR6738
0.851 0.080 1 155950962 missense variant C/A;T snv 4.3E-06 7.0E-06 5
rs5742933
ORMDL1 ; PMS1
0.882 0.080 2 189784590 5 prime UTR variant G/A;C snv 5
rs5744724
POLK
0.882 0.080 5 75599649 3 prime UTR variant G/C snv 5.4E-02 5
rs6790167
TP63
0.827 0.080 3 189869485 intron variant A/G snv 0.53 5
rs760943842
ZNF436
0.851 0.080 1 23362976 missense variant G/A snv 4.0E-05 1.4E-05 5
rs775057330
CASC1
0.851 0.080 12 25149651 missense variant C/A;T snv 5
rs775514340
CILK1
0.882 0.080 6 53041202 missense variant T/A;C snv 4.0E-06 5
rs7969931
LRMP
0.851 0.080 12 25089661 missense variant C/A;G snv 1.6E-05; 0.75 5
rs1046175
PAOX
0.851 0.080 10 133391446 stop gained C/A;G;T snv 1.2E-05; 0.88 4
rs104886026
EGFR
0.851 0.080 7 55200333 missense variant G/A snv 4
rs10519717
LOC105377462
0.851 0.080 4 144559188 intron variant T/C snv 0.21 4
rs1057519857
ERBB2 ; MIR4728
0.882 0.080 17 39724772 missense variant T/C snv 4
rs1060501327
MUTYH
0.851 0.080 1 45332251 missense variant A/G snv 4
rs11072768
CHRNB4
0.882 0.080 15 78637136 intron variant T/C;G snv 4
rs112290073
TERT
0.882 0.080 5 1285917 intron variant G/A snv 7.8E-03 4
rs11540478
IDH2
0.851 0.080 15 90085305 synonymous variant G/A;C snv 3.5E-02; 6.4E-06 4
rs1169300
HNF1A
0.882 0.080 12 120993422 intron variant G/A snv 0.27 4
rs1171287261
EGFR
0.851 0.080 7 55191839 missense variant G/A snv 4