Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs992157
TMBIM1 ; PNKD
0.790 0.080 2 218290058 5 prime UTR variant G/A snv 0.46 10
rs9879947
CD47
3 108046545 3 prime UTR variant G/A snv 0.45 1
rs976306779
AR
0.851 0.080 X 67545492 missense variant C/A;T snv 6.6E-06 8
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 11
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 15
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
rs946486
ABL1
9 130770618 intron variant C/T snv 0.44 1
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 16
rs9397080
ESR1
1.000 0.040 6 152059380 intron variant C/T snv 0.22 2
rs9350
EXO1
0.742 0.240 1 241885372 missense variant C/T snv 0.21 0.19 16
rs931127
SIPA1 ; PCNX3
0.790 0.160 11 65637829 upstream gene variant G/A snv 0.49 12
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs899706404
SDHD ; TIMM8B
0.925 0.040 11 112087944 missense variant A/G snv 3
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
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs867748453
BRAF
7 140781608 missense variant G/A snv 1
rs867114783
TP53
17 7675109 missense variant T/C snv 6
rs864622007
AR
0.882 0.200 X 67711621 missense variant T/A snv 5
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 12
rs8103851
PRKCG
0.851 0.040 19 53894400 intron variant C/G snv 0.44 5
rs79781594
RET
0.732 0.160 10 43113649 missense variant G/A;C;T snv 16
rs7977932
LRRC43 ; IL31
0.763 0.320 12 122172836 intron variant C/G;T snv 10
rs79036859
DAAM1
0.925 0.080 14 59369257 3 prime UTR variant A/G snv 3
rs781172058
CXCR4
0.732 0.320 2 136115340 synonymous variant C/T snv 4.0E-06 16