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
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
rs1057519743
CRLF2
0.827 0.120 Y 1196852 missense variant A/C snv 6
rs1057519866
NT5C2
0.851 0.120 10 103093198 missense variant C/T snv 5
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
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
rs1142345
TPMT
0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 9
rs11545078
GGH
0.807 0.200 8 63026205 missense variant G/A snv 8.8E-02 7.8E-02 6
rs1169704167
ATM
0.882 0.120 11 108284370 frameshift variant -/T delins 8.0E-06 3
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1194008138
NR3C1
0.882 0.120 5 143400121 missense variant T/C snv 4.0E-06 3
rs11978267
IKZF1
0.763 0.240 7 50398606 intron variant A/G snv 0.25 9
rs1206846668
FOLH1
0.724 0.400 11 49185773 missense variant G/A snv 4.1E-06 16
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614