Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs770795658
PGR ; PGR-AS1
11 101127788 missense variant C/T snv 6.1E-06 7.0E-06 1
rs1442033697
SERPINE1
7 101135780 frameshift variant A/- del 1
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs772903705
PSD
10 102411788 missense variant C/T snv 1
rs771086543
FBXL15 ; CUEDC2
10 102422814 missense variant G/A snv 1.3E-04 1.0E-04 1
rs11568818
MMP7
0.763 0.280 11 102530930 upstream gene variant T/A;C snv 15
rs4648068
NFKB1
0.790 0.240 4 102597148 intron variant A/G snv 0.31 9
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1200003171
AKT1
0.882 0.120 14 104775122 missense variant C/A;T snv 8.0E-06 4
rs1332018
GSTM5 ; GSTM3
0.882 0.200 1 109740350 5 prime UTR variant G/T snv 0.64 0.66 6
rs121918461
PTPN11
0.827 0.240 12 112450362 missense variant A/C;G;T snv 12
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs1213469537
CAV1
0.882 0.080 7 116559145 missense variant C/T snv 4.0E-06 1.4E-05 9
rs374733251
MET
0.882 0.080 7 116740993 missense variant A/G snv 6.0E-05 7.7E-05 5
rs56391007
MET
0.752 0.200 7 116771936 missense variant C/T snv 7.9E-03 9.0E-03 16
rs4570
UTP23 ; RAD21
0.882 0.080 8 116846150 3 prime UTR variant G/A snv 0.70 4
rs2289937
RAD21
0.882 0.080 8 116861572 intron variant G/A;C snv 4
rs4579555
RAD21
0.882 0.080 8 116867092 intron variant A/G snv 4
rs1057519788
ROS1
0.925 0.080 6 117317184 missense variant C/T snv 6
rs1927914
TLR4
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52 14
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174