Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9981660 0.882 0.080 21 42317828 upstream gene variant G/A snv 0.11 3
rs9972882
STARD3
0.925 0.080 17 39651445 intron variant A/C snv 0.66 4
rs9841504
ZBTB20
0.827 0.120 3 114643917 intron variant C/G;T snv 7
rs9589207
MIR17HG ; MIR92A1 ; MIR19B1 ; MIR20A ; MIR19A
0.925 0.080 13 91351335 mature miRNA variant G/A;C snv 5.4E-03; 4.0E-06 4
rs957201
IL36RN
0.925 0.080 2 113063623 3 prime UTR variant T/C snv 0.65 2
rs9564966 0.851 0.120 13 73322084 intergenic variant A/G snv 0.52 4
rs9502893 0.827 0.120 6 1339954 intergenic variant C/G;T snv 5
rs9471643
PGC
0.882 0.080 6 41751177 intron variant G/C snv 0.19 6
rs9426886
TRIM46
0.851 0.200 1 155179278 intron variant A/T snv 0.40 4
rs9382084
IL17F
0.925 0.080 6 52240869 intron variant G/A;T snv 2
rs937283
MDM2
0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19
rs9297976
JRK ; PSCA
0.790 0.160 8 142670817 intron variant T/C;G snv 7
rs9282861
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 31
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs911160
AURKA
0.925 0.080 20 56382507 intron variant G/A;C snv 2
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs9005
IL1RN
0.851 0.160 2 113133835 3 prime UTR variant G/A snv 0.29 4
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
rs894220185
NRP1
0.925 0.080 10 33334322 missense variant C/T snv 2
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs882537
PADI4
1.000 0.080 1 17333552 intron variant A/G snv 0.64 1
rs881844
STARD3
0.925 0.080 17 39653965 intron variant C/G snv 0.51 4
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs873601
BIVM-ERCC5 ; ERCC5
0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25