Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs895819
MIR23A ; LOC284454 ; MIR27A ; MIR24-2
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 28
rs4833095
TLR1
0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 28
rs3731249
CDKN2A
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02 23
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 22
rs2066842
NOD2
0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 15
rs1179251
IL22 ; LOC105369818
0.763 0.320 12 68251271 intron variant C/G snv 0.18 14
rs2075820
NOD1
0.790 0.200 7 30452621 missense variant C/T snv 0.27 0.28 10
rs11730582
SPP1
0.807 0.240 4 87975269 non coding transcript exon variant T/C snv 0.37 10
rs771184127
NOD2
0.790 0.200 16 50710807 missense variant G/A snv 1.2E-05 2.1E-05 9
rs13361707
PRKAA1
0.882 0.120 5 40791782 intron variant C/T snv 0.31 7
rs9841504
ZBTB20
0.827 0.120 3 114643917 intron variant C/G;T snv 7
rs199907548
CDKN2A
0.882 0.160 9 21974682 missense variant A/C;G snv 6.3E-04 5
rs11730059 0.925 0.120 4 87966175 intergenic variant A/G snv 0.93 4
rs718226
LOC102724907
0.882 0.120 16 50735652 intron variant A/G snv 0.36 4
rs2709800
NOD1
0.882 0.120 7 30473155 intron variant A/C snv 0.53 4
rs2853744
SPP1
0.882 0.200 4 87975096 non coding transcript exon variant G/T snv 0.14 4
rs10505799 1.000 0.040 12 16293334 intergenic variant T/C snv 0.10 2
rs6878265 1.000 0.040 5 120069960 intergenic variant C/T snv 0.29 2
rs1042194
CYP2C18
1.000 0.040 10 94735727 3 prime UTR variant G/C;T snv 2
rs6833161 4 87968453 intergenic variant T/C snv 0.47 1