Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10106
FPGS
0.851 0.200 9 127813796 3 prime UTR variant T/C snv 0.45 4
rs10235796
IKZF1
0.882 0.120 7 50394939 intron variant T/C snv 0.82 3
rs10272724 0.882 0.200 7 50409515 downstream gene variant T/C snv 0.24 4
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104893636
HOXD4 ; HOXD3
0.882 0.120 2 176151875 missense variant A/C;T snv 5.2E-06; 7.9E-04 3
rs1051296
SLC19A1
0.882 0.120 21 45514947 3 prime UTR variant A/C snv 0.43 0.44 3
rs10519612
IL15
0.882 0.120 4 141732548 intron variant A/C snv 0.10 3
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519743
CRLF2
0.827 0.120 Y 1196852 missense variant A/C snv 6
rs1057519753
JAK1
0.763 0.120 1 64846664 missense variant C/A snv 9
rs1057519773
ABL1
0.851 0.160 9 130872901 missense variant T/A;C;G snv 4
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs1057519866
NT5C2
0.851 0.120 10 103093198 missense variant C/T snv 5
rs10740055
ARID5B
0.790 0.240 10 61958720 intron variant C/A snv 0.49 7
rs10821936
ARID5B
0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs10828317
PIP4K2A
0.776 0.280 10 22550699 missense variant T/C snv 9
rs10853104
IGF2BP1
1.000 0.120 17 49014714 intron variant C/G;T snv 1
rs10994982
ARID5B
0.790 0.120 10 61950345 intron variant A/G snv 0.49 7
rs11099592
HPSE
0.851 0.160 4 83309466 missense variant T/C snv 0.78 0.80 5
rs111033563
LOC108783645 ; HFE
0.776 0.240 6 26092916 missense variant A/C snv 4.0E-06 8
rs111978267
KCNQ1
0.882 0.120 11 2751648 intron variant C/G;T snv 2.8E-05 3
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214