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
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
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
rs1801265
DPYD
0.763 0.280 1 97883329 missense variant A/G snv 0.28 13
rs2239633
CEBPE
0.742 0.240 14 23119848 upstream gene variant G/A snv 0.38 12
rs10821936
ARID5B
0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs3824662
GATA3
0.752 0.320 10 8062245 intron variant C/A;T snv 11
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 10
rs3731217
CDKN2A
0.763 0.320 9 21984662 intron variant A/C;T snv 10
rs7089424
ARID5B
0.752 0.200 10 61992400 intron variant T/G snv 0.32 10
rs1057519753
JAK1
0.763 0.120 1 64846664 missense variant C/A snv 9
rs11978267
IKZF1
0.763 0.240 7 50398606 intron variant A/G snv 0.25 9
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 9
rs4132601
IKZF1
0.763 0.240 7 50402906 3 prime UTR variant T/G snv 0.25 9
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 8
rs1966862
ARHGAP24
0.790 0.120 4 85766908 intron variant A/G snv 0.14 8
rs10740055
ARID5B
0.790 0.240 10 61958720 intron variant C/A snv 0.49 7