Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1139
ZNF385B
0.851 0.200 2 179745354 intron variant C/T snv 0.22 4
rs6757845
ZNF385B
0.851 0.200 2 179449268 intron variant T/C snv 0.66 4
rs117496742
YAP1
1.000 0.120 11 102208982 intron variant G/A;T snv 1.3E-02 1
rs7205289
WWP2 ; MIR140
0.882 0.200 16 69933102 non coding transcript exon variant C/A snv 3
rs201002930
WNT10A
0.827 0.200 2 218889997 synonymous variant C/T snv 3.2E-05 7.0E-06 6
rs1487022
VPS13B
0.925 0.120 8 99517598 intron variant G/T snv 0.17 2
rs957448
VIRMA
0.925 0.120 8 94529074 synonymous variant A/G;T snv 0.33 2
rs6585429
VAX1
0.925 0.120 10 117133720 3 prime UTR variant A/G snv 0.68 2
rs2289187
UBL7
0.925 0.120 15 74452058 intron variant C/T snv 0.24 2
rs76479869
TP63
0.882 0.120 3 189835583 intron variant C/T snv 4.3E-02 3
rs2304269
TMEM19
0.925 0.120 12 71686492 5 prime UTR variant T/C snv 6.5E-02 2
rs11582254
TMCO4
0.925 0.120 1 19691584 intron variant T/A;C snv 2
rs8179096
TIMP2
0.851 0.200 17 78925567 upstream gene variant G/A;C snv 4
rs104893810
TGFBR2
0.790 0.360 3 30691477 missense variant C/T snv 7
rs11466285
TGFA
0.851 0.200 2 70450307 3 prime UTR variant A/C;G snv 5
rs2166975
TGFA
0.827 0.240 2 70450862 synonymous variant G/A snv 0.24 0.23 5
rs3771523
TGFA
0.851 0.200 2 70450336 3 prime UTR variant C/T snv 0.14 5
rs1588366
TANC2
0.925 0.120 17 62999067 regulatory region variant A/G snv 0.23 2
rs189675673
SULT2A1
1.000 0.120 19 47880143 intron variant G/A;T snv 1
rs62529857
SULT2A1
1.000 0.120 19 47883216 intron variant T/C snv 7.7E-03 1
rs11774066
STK3
0.925 0.120 8 98443083 intron variant C/T snv 0.20 2
rs140291094
STAC3
0.742 0.320 12 57244322 missense variant C/G snv 9.1E-05 3.8E-04 11
rs739439
SLC46A1 ; SARM1
0.851 0.200 17 28396803 3 prime UTR variant C/T snv 0.13 5
rs10133673
SLC25A21
0.925 0.120 14 37068147 intron variant T/C snv 2.8E-02 2
rs146753226
SIX2
0.882 0.200 2 45006255 missense variant C/T snv 1.1E-04 4.0E-04 3