Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 10
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 10
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 10
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 9
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 9
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 9
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 9
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 8
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 8
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 8
rs3741378
SIPA1
0.851 0.080 11 65641466 missense variant C/G;T snv 0.15 8
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 7
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 7
rs3110697
IGFBP3
0.827 0.160 7 45915430 intron variant A/G snv 0.58 7
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 7
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 7