Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs360719
IL18 ; LOC107987164 ; TEX12
0.790 0.480 11 112165426 non coding transcript exon variant A/G snv 0.25 7
rs11039155
NR1H3
0.827 0.400 11 47259211 5 prime UTR variant G/A snv 0.14 0.12 6
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs2297235
GSTO2
0.752 0.320 10 104274733 5 prime UTR variant A/G snv 0.22 11
rs7069102
SIRT1
0.790 0.440 10 67903362 intron variant C/G snv 0.64 10
rs2273773
SIRT1
0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 9
rs2281997
ENHO
0.882 0.240 9 34521869 intron variant T/A;C snv 5
rs10881578
RXRA
0.925 0.240 9 134340689 intron variant A/G snv 0.32 2
rs9657182
IDO1
0.851 0.280 8 39908329 intron variant C/G;T snv 6
rs2292779
AGO2
0.851 0.320 8 140551294 intron variant G/C;T snv 0.57; 4.9E-06 4
rs1805323
PMS2
0.925 0.160 7 5987311 missense variant G/A;T snv 4.0E-06; 8.0E-02 2
rs12668183 1.000 0.120 7 16455781 regulatory region variant T/C snv 0.34 1
rs756573441
CALD1
1.000 0.120 7 134933359 missense variant A/G;T snv 4.2E-06 1
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs4746
GLO1
0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21
rs73786719
ADGB
1.000 0.120 6 146716848 intron variant C/A snv 1.7E-02 3.3E-02 1
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs10719
DROSHA
0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs644236
DROSHA
0.882 0.320 5 31409008 non coding transcript exon variant T/C snv 0.31 0.35 5
rs557874766
MSH3 ; DHFR
0.925 0.160 5 80654926 missense variant C/G;T snv 8.5E-06; 6.8E-05; 8.5E-06 2
rs1232027
LINC01337
1.000 0.120 5 80619201 intron variant G/A snv 0.32 1
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59