Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6479778
ARID5B
0.827 0.200 10 61929318 intron variant T/C;G snv 5
rs1057519773
ABL1
0.851 0.160 9 130872901 missense variant T/A;C;G snv 4
rs121913451
ABL1
0.851 0.160 9 130872903 missense variant C/A;G snv 4
rs766639320
CLTA
0.851 0.240 9 36211617 missense variant C/G snv 4.0E-06 4
rs121909646
FLT3
0.882 0.120 13 28018504 missense variant T/A;G snv 3
rs12540874
GRB10
0.882 0.280 7 50597225 intron variant A/C;G snv 3
rs4463516 1.000 0.120 9 32867483 intron variant G/C;T snv 3
rs4896310
LOC105378021
1.000 0.120 6 138018697 intergenic variant A/G;T snv 3
rs72772090
CAST
1.000 0.120 5 96700607 intron variant G/A;C snv 3
rs7818688
NDUFAF6
1.000 0.120 8 95011854 intron variant C/A;G snv 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
rs1339159756
INSL6 ; JAK2
0.925 0.120 9 5078395 missense variant C/G snv 2
rs398123063
LOC105376032 ; PAX5
0.925 0.120 9 37002705 missense variant C/T snv 2
rs6944602 0.925 0.120 7 50406053 downstream gene variant G/A;T snv 2
rs10261922 1.000 0.120 7 50414314 intergenic variant C/A;G;T snv 1
rs10899736
DDC ; FIGNL1
1.000 0.120 7 50479227 intron variant G/A;C snv 1
rs1110701 1.000 0.120 7 50410929 intergenic variant A/G;T snv 1
rs112141546
ADAMTS18
1.000 0.120 16 77367618 missense variant C/A;G;T snv 4.0E-06; 1.4E-03 1
rs11575387
FIGNL1 ; DDC
1.000 0.120 7 50499737 intron variant T/A;G snv 1
rs17079534 1.000 0.120 3 39805581 upstream gene variant G/A;C snv 1
rs1945213 1.000 0.120 11 56408195 upstream gene variant C/G;T snv 1
rs2069426
CDKN2B ; CDKN2B-AS1
1.000 0.120 9 22006274 intron variant G/A;C;T snv 4.4E-06; 4.4E-06; 7.5E-02 1
rs207954
SLCO3A1
1.000 0.120 15 92114143 intron variant T/A;C;G snv 1
rs2622849
COL11A1
1.000 0.120 1 102955788 intron variant T/A;C;G snv 1