Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9966483
LOC643542
0.925 0.160 18 67783109 intron variant G/A;T snv 2
rs9958800
PHLPP1 ; LOC105372160
0.925 0.160 18 62773567 intron variant T/A snv 0.25 2
rs994411260
DNMT1
0.925 0.160 19 10194877 missense variant G/C snv 2
rs9942471 0.925 0.160 6 89238513 intergenic variant A/C snv 0.37 2
rs9674559
RPTOR
0.925 0.160 17 80741808 intron variant A/G snv 0.22 2
rs955333 0.882 0.240 6 154626274 intergenic variant A/G snv 0.13 3
rs9533481
ENOX1
1.000 0.120 13 43415049 intron variant T/C snv 0.78 1
rs953239
TRPC1
1.000 0.120 3 142727363 intron variant A/C snv 0.46 1
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs852426
ACTB
0.882 0.240 7 5526722 downstream gene variant C/T snv 0.39 5
rs841853
SLC2A1
0.882 0.200 1 42935767 intron variant A/C snv 0.66 4
rs838136
FUT1
1.000 0.120 19 48753131 intron variant T/C snv 0.41 1
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs8192678
PPARGC1A
0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs805304
CLIC1 ; DDAH2
0.851 0.240 6 31730311 5 prime UTR variant T/G snv 0.48 5
rs80356814
LMNA
0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 15
rs7916840
GPR158
0.925 0.160 10 25424152 intron variant A/T snv 0.70 2
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs7782979
ELMO1
0.925 0.160 7 36865445 intron variant C/A snv 0.46 2
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs770917264
MOK
1.000 0.120 14 102229547 stop gained G/A;C snv 4.0E-06; 1.6E-05 1
rs7679
PCIF1
0.925 0.160 20 45947863 3 prime UTR variant T/C snv 0.13 9
rs765798193
PSMD9
0.732 0.320 12 121915884 frameshift variant G/-;GG delins 18
rs7639705
MCF2L2
1.000 0.120 3 183309754 missense variant T/G snv 0.26 0.27 1
rs7638459
TRPC1
1.000 0.120 3 142771309 intron variant T/C snv 0.35 1