Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10049390
SLCO2A1
0.776 0.080 3 133982275 intron variant G/A snv 0.67 10
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 22
rs10152518 0.790 0.080 15 67884824 intergenic variant G/A;T snv 9
rs1017621656
TGFB1
0.925 0.080 19 41352923 missense variant A/C;G snv 1.9E-05 3
rs1021631442
FBXO11 ; MSH6
0.882 0.200 2 47806279 missense variant G/A snv 3
rs10222633
CASR
0.925 0.080 3 122258079 intron variant G/A snv 0.45 4
rs1028166
TENM3 ; TENM3-AS1
0.790 0.080 4 181892145 intron variant G/A snv 0.74 9
rs1035209 0.790 0.080 10 99585609 intergenic variant C/T snv 0.15 9
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs10411210
RHPN2
0.742 0.160 19 33041394 intron variant C/T snv 0.22 13
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs1042821
MSH6
0.732 0.280 2 47783349 missense variant G/A;C;T snv 0.18; 8.6E-06 16
rs1044129
AVEN ; RYR3
0.790 0.200 15 33866065 3 prime UTR variant A/G;T snv 9
rs10450310
MBL2
0.925 0.080 10 52764898 downstream gene variant G/A snv 0.29 2
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10457678
ECT2L
0.790 0.080 6 138801103 intron variant A/G snv 0.19 10
rs104894226
LRRC56 ; HRAS
0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 16
rs10511330
ZBTB20
0.776 0.080 3 114402172 intron variant T/C snv 0.22 10
rs1051753269
EGFR
0.790 0.120 7 55174029 missense variant G/A snv 7.0E-06 7
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147