Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs116909374 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 11
rs12508721
IL21-AS1
0.742 0.360 4 122623509 intron variant C/T snv 0.24 11
rs2060793
CYP2R1
0.776 0.240 11 14893764 upstream gene variant A/G snv 0.63 11
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 11
rs1867277
PTCSC2 ; FOXE1
0.776 0.160 9 97853632 5 prime UTR variant A/G snv 0.63 10
rs2439302
NRG1
0.776 0.200 8 32574851 intron variant G/C snv 0.54 9
rs1443438
PTCSC2
0.827 0.080 9 97787746 intron variant T/A;C snv 8
rs17849071
PIK3CA
0.776 0.160 3 179218439 intron variant T/G snv 7.9E-02 8
rs3783521
IL1A
0.807 0.200 2 112786000 upstream gene variant G/A snv 0.26 8
rs56062135
SMAD3
0.790 0.200 15 67163292 intron variant C/T snv 0.18 8
rs1064795638
BAP1
0.851 0.080 3 52403251 stop gained G/A snv 7
rs6013897 0.790 0.200 20 54125940 regulatory region variant T/A snv 0.23 7
rs121913308
RET
0.827 0.120 10 43114492 missense variant A/C;G;T snv 6
rs2245214
ATG5
0.827 0.240 6 106214866 intron variant C/G snv 0.42 6
rs3917225
IL1R1
0.807 0.160 2 102152842 intron variant A/G snv 0.36 6
rs768827923
PIK3CD
0.851 0.080 1 9721816 missense variant T/G snv 6
rs7850258
PTCSC2
0.827 0.200 9 97786731 intron variant A/G snv 0.72 6
rs925489
PTCSC2
0.882 0.080 9 97784318 intron variant C/T snv 0.71 6
rs360718
IL18
0.827 0.120 11 112164016 5 prime UTR variant A/C snv 0.26 5
rs786203472
CHEK2
0.827 0.120 22 28719414 start lost T/C snv 5
rs863224748
CHEK2
0.827 0.120 22 28734721 start lost T/C snv 5
rs10759944
PTCSC2
0.925 0.080 9 97794690 intron variant A/G snv 0.72 4
rs1248131654
RBMS1
0.851 0.080 2 160367217 missense variant G/A snv 1.4E-05 4
rs13143866
IL21 ; IL21-AS1
0.851 0.200 4 122619603 intron variant G/A snv 0.24 4
rs1443434
FOXE1
0.851 0.080 9 97855197 3 prime UTR variant G/T snv 0.63 4