Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2747648
ESR1
0.925 0.080 6 152101200 3 prime UTR variant C/T snv 0.98 2
rs56333866
PIP4K2A
1.000 0.080 10 22581150 intron variant TTTC/- delins 0.97 1
rs132390
LOC105372985 ; EMID1
0.925 0.080 22 29225488 intron variant C/T snv 0.96 2
rs828200 0.925 0.080 13 90718206 regulatory region variant C/T snv 0.96 2
rs2206593
PTGS2
0.925 0.080 1 186673297 3 prime UTR variant A/G snv 0.95 3
rs4896011
TCF21
0.925 0.080 6 133893615 3 prime UTR variant A/T snv 0.94 2
rs4759314
HOTAIR
0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs1189020
LINC02284
1.000 0.080 14 56410241 intron variant T/G snv 0.93 1
rs11085735
KEAP1
0.925 0.080 19 10491504 intron variant A/C snv 0.92 2
rs1801726
CASR
0.732 0.280 3 122284985 missense variant G/C snv 0.95 0.92 13
rs2665390
LOC107986148 ; TIPARP
0.776 0.160 3 156679960 intron variant C/T snv 0.92 8
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs861529
XRCC3 ; KLC1
0.925 0.080 14 103712977 3 prime UTR variant T/C snv 0.91 2
rs1858826
GNGT1
1.000 0.080 7 93719703 intron variant C/T snv 0.90 3
rs1230666
MAGI3
0.925 0.200 1 113630788 intron variant A/G snv 0.90 2
rs7558475
CFLAR
0.925 0.080 2 201171755 3 prime UTR variant G/A snv 0.90 2
rs6453204
SV2C
1.000 0.080 5 76143375 intron variant A/G snv 0.90 2
rs7766238
TCF21
0.925 0.080 6 133893438 3 prime UTR variant A/G snv 0.90 2
rs6556756
LOC105377703 ; LINC02143
0.882 0.160 5 164462274 intron variant G/T snv 0.89 3
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs1802904
XRN1 ; ATR
0.925 0.080 3 142449489 synonymous variant C/T snv 0.86 0.89 2
rs1952246
RAD51B ; LOC105370546
1.000 0.080 14 68165095 intron variant G/A snv 0.89 1
rs1958115
RAD51B
1.000 0.080 14 68170948 intron variant C/A snv 0.89 1
rs198580
RB1
0.925 0.080 13 48459611 intron variant G/A snv 0.89 2
rs1675126
INCENP
0.925 0.080 11 62138902 synonymous variant T/C snv 0.84 0.88 3