Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10017134
UGT2A2 ; UGT2A1
0.925 0.120 4 69591303 intron variant T/C snv 0.75 2
rs1002076
KIF1B
0.925 0.120 1 10378834 3 prime UTR variant G/A snv 0.33 2
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13 4
rs1017134 0.925 0.120 7 35307237 intergenic variant G/A snv 0.47 2
rs10260419
THSD7A
0.882 0.120 7 11524758 intron variant C/G snv 0.26 3
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1057156
RUVBL1
0.925 0.120 3 128081228 3 prime UTR variant A/G snv 0.22 0.23 2
rs10788679
ARHGEF10L
0.925 0.120 1 17590467 intron variant A/G snv 0.59 2
rs11175194
SRGAP1
0.925 0.120 12 63871057 intron variant G/A snv 0.15 2
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs114972508
EGFR ; LOC105375284
0.925 0.120 7 55020815 intron variant T/C snv 1.4E-02 2
rs115344852
GPX6
1.000 0.120 6 28518321 intron variant A/C snv 1
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52 9
rs11696662
PLCG1
0.925 0.120 20 41161795 intron variant C/T snv 4.4E-02 2
rs11782652
CHMP4C
0.851 0.120 8 81741409 intron variant A/G snv 6.6E-02 4
rs1192691 0.925 0.120 10 36880367 regulatory region variant G/T snv 0.90 2
rs12039431
RSPO1
1.000 0.120 1 37616450 intron variant G/A snv 0.24 0.21 1
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62