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
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs7089424
ARID5B
0.752 0.200 10 61992400 intron variant T/G snv 0.32 10
rs4132601
IKZF1
0.763 0.240 7 50402906 3 prime UTR variant T/G snv 0.25 9
rs1142345
TPMT
0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 9
rs140422742
CYP3A4
0.882 0.120 7 99778046 missense variant T/C;G snv 7.6E-05 6.3E-05 3
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs564398
CDKN2B-AS1
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 18
rs16754
WT1
0.732 0.240 11 32396399 synonymous variant T/C snv 0.24; 4.0E-06 0.17 15
rs2536
MTOR
0.776 0.240 1 11106656 3 prime UTR variant T/C snv 5.8E-02 11
rs10828317
PIP4K2A
0.776 0.280 10 22550699 missense variant T/C snv 9
rs11099592
HPSE
0.851 0.160 4 83309466 missense variant T/C snv 0.78 0.80 5
rs10106
FPGS
0.851 0.200 9 127813796 3 prime UTR variant T/C snv 0.45 4
rs17007695 0.851 0.120 4 141788570 intergenic variant T/C snv 7.7E-02 4
rs7789635 0.882 0.120 7 50405912 downstream gene variant T/C snv 0.40 4
rs786205155
ETV6
0.882 0.120 12 11884481 missense variant T/C snv 4
rs10235796
IKZF1
0.882 0.120 7 50394939 intron variant T/C snv 0.82 3
rs1194008138
NR3C1
0.882 0.120 5 143400121 missense variant T/C snv 4.0E-06 3
rs1361742125
NR3C1
0.882 0.120 5 143399842 missense variant T/C snv 4.0E-06 7.0E-06 3
rs1412792500
NR3C1
0.882 0.120 5 143400541 missense variant T/C snv 4.0E-06 1.4E-05 3
rs1573613
ETV6
0.882 0.120 12 11894684 3 prime UTR variant T/C snv 0.48 3
rs3794012
LMO1
0.882 0.120 11 8248697 intron variant T/C snv 0.32 3
rs4237770
LMO1
0.882 0.120 11 8254288 intron variant T/C snv 0.37 3