Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1141718
SOD2
0.724 0.280 6 159688224 missense variant A/G snv 15
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs1805105
AXIN1
0.776 0.280 16 346264 synonymous variant A/G snv 0.61 0.69 11
rs12628
LRRC56 ; HRAS
0.776 0.160 11 534242 synonymous variant A/G snv 0.32 0.34 10
rs3731239
CDKN2A
0.763 0.240 9 21974219 intron variant A/G snv 0.26 10
rs709816
NBN
0.752 0.320 8 89955483 synonymous variant A/G snv 0.47 0.51 10
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs9288518
XRCC5
0.776 0.240 2 216196997 intron variant A/G snv 0.35 9
rs1883965
MTOR
0.807 0.160 1 11262099 intron variant A/G snv 0.63 8
rs8679
PARP1
0.790 0.200 1 226360853 3 prime UTR variant A/G snv 0.16 7
rs778990691
CCNH
0.807 0.240 5 87395069 missense variant A/G snv 4.0E-06 6
rs7211818
RPTOR
0.827 0.200 17 80715103 intron variant A/G snv 0.23 5
rs1484761909
GSTM1 ; GSTM2
0.882 0.120 1 109688224 missense variant A/G snv 3.0E-05 3.8E-05 3
rs6464268 0.882 0.120 7 152684065 intergenic variant A/G snv 0.23 3
rs1937920 0.925 0.120 10 5119763 downstream gene variant A/G snv 0.28 2
rs1258767
FMN1
1.000 0.120 15 32834253 intron variant A/G snv 0.18 1
rs121913279
PIK3CA
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs2234922
EPHX1
0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs156697
GSTO2
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs10719
DROSHA
0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs2306283
SLCO1B1
0.742 0.320 12 21176804 missense variant A/G;T snv 0.47 16
rs2230641
CCNH
0.807 0.240 5 87399457 missense variant A/G;T snv 0.18 0.17 8
rs9034
NAMPT
0.827 0.200 7 106249610 3 prime UTR variant A/G;T snv 5
rs1135612
POR
0.882 0.120 7 75980359 synonymous variant A/G;T snv 0.28 3
rs140241283
MTHFR
0.882 0.120 1 11796249 start lost A/G;T snv 4.0E-06; 4.0E-06 3