Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3781093
GATA3
0.882 0.120 10 8059964 intron variant T/C snv 0.19 3
rs3794845
MBP
0.882 0.120 18 77002561 intron variant G/C snv 0.12 3
rs41307935
ZDHHC18
1.000 0.120 1 26854576 3 prime UTR variant C/T snv 6.1E-02 3
rs4245555
GRB10
1.000 0.120 7 50593712 intron variant T/C snv 0.32 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
rs637868
PHGDH
1.000 0.120 1 119714487 splice region variant T/C snv 0.56 3
rs6550253
LINC01811
1.000 0.120 3 34149739 intron variant G/A snv 0.12 3
rs6684897 1.000 0.120 1 238128048 intergenic variant C/G snv 0.83 3
rs72772090
CAST
1.000 0.120 5 96700607 intron variant G/A;C snv 3
rs74709575
LINC02334
1.000 0.120 13 38041119 intron variant A/C snv 3.1E-03 3
rs7818688
NDUFAF6
1.000 0.120 8 95011854 intron variant C/A;G snv 3
rs920590 1.000 0.120 8 19793650 regulatory region variant T/C snv 0.39 3
rs10821938
ARID5B
0.925 0.120 10 61965014 intron variant A/C snv 0.56 2
rs11770117 1.000 0.120 7 50406065 downstream gene variant A/T snv 0.41 2
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
rs12719019 1.000 0.120 7 50408441 downstream gene variant C/T snv 0.40 2
rs1339159756
INSL6 ; JAK2
0.925 0.120 9 5078395 missense variant C/G snv 2
rs147390019
NUDT15
0.925 0.120 13 48045720 missense variant G/A snv 2.6E-03 2.2E-03 2
rs2242041
FIGNL1 ; DDC
0.925 0.120 7 50461751 intron variant C/G snv 7.7E-02 2
rs3887825
DDC ; FIGNL1
1.000 0.120 7 50477395 intron variant T/C snv 0.56 2
rs398123063
LOC105376032 ; PAX5
0.925 0.120 9 37002705 missense variant C/T snv 2
rs408626
DHFR ; MSH3
0.925 0.120 5 80655314 non coding transcript exon variant T/C snv 0.48 2
rs442767
MSH3 ; DHFR
0.925 0.120 5 80655677 intron variant G/T snv 0.27 2