Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7075634
PIP4K2A
1.000 0.120 10 22564173 intron variant T/C snv 0.57 1
rs4982729 1.000 0.120 14 23107402 upstream gene variant T/C snv 0.66 1
rs12887958 1.000 0.120 14 23113360 downstream gene variant C/T snv 0.37 1
rs4982731 1.000 0.120 14 23116124 downstream gene variant C/T snv 0.68 1
rs8015478
CEBPE
1.000 0.120 14 23116809 downstream gene variant A/C snv 0.68 2
rs2239633
CEBPE
0.742 0.240 14 23119848 upstream gene variant G/A snv 0.38 12
rs6684897 1.000 0.120 1 238128048 intergenic variant C/G snv 0.83 3
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs60218192
HS3ST4
1.000 0.120 16 25874649 intron variant G/A;C snv 8.6E-02 1
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 8
rs41307935
ZDHHC18
1.000 0.120 1 26854576 3 prime UTR variant C/T snv 6.1E-02 3
rs121913232
FLT3
0.925 0.120 13 28018500 missense variant G/C snv 2
rs121913487
FLT3
0.925 0.120 13 28018503 missense variant A/C;T snv 2
rs121909646
FLT3
0.882 0.120 13 28018504 missense variant T/A;G snv 3
rs121913488
FLT3
0.807 0.120 13 28018505 missense variant C/A;G;T snv 7
rs17855750
IL27
0.695 0.480 16 28503907 missense variant A/C;T snv 6.4E-02; 4.0E-06 21
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs147481775
DEPDC5
1.000 0.120 22 31829377 intron variant C/A snv 6.6E-03 3
rs16754
WT1
0.732 0.240 11 32396399 synonymous variant T/C snv 0.24; 4.0E-06 0.17 15
rs4463516 1.000 0.120 9 32867483 intron variant G/C;T snv 3
rs6550253
LINC01811
1.000 0.120 3 34149739 intron variant G/A snv 0.12 3
rs766639320
CLTA
0.851 0.240 9 36211617 missense variant C/G snv 4.0E-06 4
rs398123063
LOC105376032 ; PAX5
0.925 0.120 9 37002705 missense variant C/T snv 2
rs74709575
LINC02334
1.000 0.120 13 38041119 intron variant A/C snv 3.1E-03 3