Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs705382
PON1
0.827 0.200 7 95325909 upstream gene variant C/G snv 0.53 5
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs61886277
PLCE1
1.000 0.080 10 94012060 intergenic variant C/T snv 0.19 1
rs7712322
POLR3G
1.000 0.080 5 90482078 intron variant C/A;T snv 1
rs11556218
IL16
0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs7813
GEMIN4
0.689 0.360 17 744946 missense variant G/A;C snv 0.63 22
rs2296651
SLC10A1
0.732 0.240 14 69778476 missense variant G/A snv 6.3E-03 2.5E-03 13
rs2132039
UGT2B28
0.925 0.120 4 69293669 intron variant T/A;C snv 2
rs1353702185
MDM2
0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs11465817
IL23R
0.882 0.120 1 67255414 intron variant C/A;T snv 4
rs1884444
IL23R ; C1orf141
0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 34
rs12354
LTBR
0.925 0.080 12 6390939 3 prime UTR variant T/A;G snv 1.6E-04; 0.76 2
rs3759333
LTBR
0.882 0.120 12 6382781 intron variant C/G;T snv 3
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs7095891
MBL2
0.882 0.120 10 52771701 upstream gene variant G/A snv 0.30 3
rs4935047
MBL2
1.000 0.080 10 52770307 intron variant A/G snv 0.49 1
rs6715787
EPAS1
0.851 0.200 2 46349033 intron variant C/G;T snv 4
rs13419896
EPAS1
0.776 0.240 2 46329206 intron variant G/A snv 0.10 8
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1010023
PNPLA3
0.851 0.080 22 43940218 intron variant T/C snv 0.20 4
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs2293152
STAT3
0.763 0.480 17 42329511 intron variant G/A;C;T snv 2.8E-05; 0.59; 1.6E-05 10