Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs9470794
ZFAND3
0.925 0.080 6 38139068 intron variant T/C snv 0.12 3
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs17118
XYLB
0.925 0.120 3 38362981 missense variant C/A;T snv 0.29 4
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs734312
WFS1
0.790 0.240 4 6301627 missense variant G/A snv 0.55 0.42 10
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs752854
WFS1
0.925 0.080 4 6280234 intron variant C/G;T snv 3
rs1906436
WDR72
1.000 0.040 15 53590245 intron variant T/C snv 0.32 3
rs12522383
WDR36
5 111119568 intron variant G/A snv 0.29 2
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs9677
VIPR1
0.925 0.080 3 42537370 3 prime UTR variant C/T snv 0.39 3
rs17697515
VEGFC ; LOC105377555
1.000 0.080 4 176689270 intron variant C/T snv 5.1E-02 2
rs2333526
VEGFC
1.000 0.080 4 176782151 intron variant T/A;C snv 2
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs3025039
VEGFA
0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2239179
VDR
0.790 0.200 12 47863983 intron variant T/C snv 0.39 9
rs7528153
VAV3
0.925 0.080 1 107765105 missense variant T/A snv 0.58 0.64 4
rs2890565
UTS2
0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 15
rs228648
UTS2
0.776 0.360 1 7853370 missense variant G/A snv 0.51 0.52 13