Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs121913682
KIT
0.605 0.400 4 54733167 missense variant A/G;T snv 52
rs2430561
IFNG ; IFNG-AS1
0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 49
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs397507520
PTPN11
0.658 0.520 12 112453279 missense variant G/C;T snv 39
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs368087026
SLC19A1
0.637 0.520 21 45530890 missense variant G/A snv 33
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs4553808
CTLA4
0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs121913459
ABL1
0.672 0.160 9 130872896 missense variant C/T snv 25
rs57095329
MIR3142HG
0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv 23
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs2295080
MTOR
0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs2735383
OSGIN2 ; NBN
0.708 0.360 8 89935041 3 prime UTR variant C/G snv 0.31 18
rs1801265
DPYD
0.763 0.280 1 97883329 missense variant A/G snv 0.28 13