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
rs16998248
ZNF217
0.882 0.040 20 53581801 synonymous variant T/A snv 0.11 8.8E-02 3
rs35720349
ZNF217
0.882 0.040 20 53577121 missense variant G/A snv 3.4E-02 1.6E-02 3
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs16971436
ZFHX3
0.851 0.080 16 72958864 missense variant T/C;G snv 1.2E-05; 7.1E-02 4
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs7819412
XKR6
0.827 0.120 8 11187652 intron variant G/A;T snv 6
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs216311
VWF
0.882 0.040 12 6019277 missense variant T/A;C snv 4.0E-06; 0.69 7
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1010
VAMP8
0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
rs2516839
USF1
0.732 0.320 1 161043331 5 prime UTR variant C/T snv 0.49 14
rs660339
UCP2
0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs7211
TXNIP
0.827 0.200 1 145993449 3 prime UTR variant G/A;C;T snv 6
rs7212
TXNIP
0.851 0.120 1 145992816 3 prime UTR variant G/C snv 0.16 5
rs756601757
TSTD1 ; USF1
0.882 0.040 1 161040847 missense variant G/A snv 8.0E-06 3
rs972655070
TSTD1 ; USF1
0.882 0.040 1 161040282 missense variant G/A snv 4.0E-06 1.4E-05 3
rs2295490
TRIB3
0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs2453021
TNFRSF9
0.807 0.080 1 7929506 intron variant C/A;T snv 6