Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16754
WT1
0.732 0.240 11 32396399 synonymous variant T/C snv 0.24; 4.0E-06 0.17 15
rs1801265
DPYD
0.763 0.280 1 97883329 missense variant A/G snv 0.28 13
rs116855232
NUDT15
0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 12
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
rs738408
PNPLA3
0.925 0.120 22 43928850 synonymous variant C/T snv 0.28 0.22 10
rs1057519753
JAK1
0.763 0.120 1 64846664 missense variant C/A snv 9
rs1142345
TPMT
0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 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
rs10994982
ARID5B
0.790 0.120 10 61950345 intron variant A/G snv 0.49 7
rs1135401746
GNB1
0.827 0.400 1 1806512 missense variant C/G snv 7
rs121913488
FLT3
0.807 0.120 13 28018505 missense variant C/A;G;T snv 7
rs924607
LOC105374608 ; LOC100996325
0.851 0.120 5 609978 intron variant C/T snv 0.32 7
rs387906517
ABL1
0.827 0.120 9 130862919 missense variant G/A snv 6
rs121913448
ABL1
0.827 0.120 9 130862976 missense variant G/A snv 5
rs2036914
F11
0.882 0.160 4 186271327 intron variant T/C snv 0.57 5