Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9557635
NALCN
1.000 0.040 13 101398739 intron variant A/G snv 0.70 1
rs193100333
YAP1
1.000 0.040 11 102209523 missense variant C/T snv 3.0E-04 1.1E-04 1
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs11591710 0.882 0.160 10 103927874 intergenic variant A/C snv 0.16 3
rs190996050 1.000 0.040 5 1048492 downstream gene variant T/C snv 5.7E-03 1
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs78442819
TEKT5
1.000 0.040 16 10647125 intron variant G/C snv 0.13 2
rs189037
ATM ; NPAT
0.689 0.400 11 108223106 5 prime UTR variant G/A snv 0.49 22
rs879254046
ATM
0.925 0.240 11 108267246 stop gained G/A;C;T snv 2
rs611646
ATM
0.882 0.120 11 108306370 intron variant T/A;C snv 3
rs745775382
ATM ; C11orf65
1.000 0.040 11 108333954 missense variant A/C;G snv 8.0E-06 1
rs879254065
ATM ; C11orf65
1.000 0.040 11 108345849 missense variant C/G snv 1
rs3827760
RANBP2 ; EDAR
0.752 0.160 2 108897145 missense variant A/G snv 0.15 5.9E-02 11
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs397507546
PTPN11
0.790 0.360 12 112489084 missense variant G/A;C;T snv 9
rs7086803
VTI1A
0.763 0.160 10 112738717 intron variant G/A snv 0.20 9
rs121913331
APC
0.851 0.120 5 112838934 stop gained C/A;T snv 8.0E-06 11
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs26538
ATG12 ; AP3S1
1.000 0.040 5 115842698 intron variant C/T snv 0.44 1
rs1484038087
ROS1
1.000 0.040 6 117317181 missense variant C/T snv 4.0E-06 1
rs1057519788
ROS1
0.925 0.080 6 117317184 missense variant C/T snv 6
rs6942067
DCBLD1
1.000 0.040 6 117464533 intron variant A/G snv 0.38 1
rs9387478
DCBLD1
0.851 0.080 6 117465017 intron variant C/A;T snv 4