Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1966862
ARHGAP24
0.790 0.120 4 85766908 intron variant A/G snv 0.14 8
rs10994982
ARID5B
0.790 0.120 10 61950345 intron variant A/G snv 0.49 7
rs924607
LOC105374608 ; LOC100996325
0.851 0.120 5 609978 intron variant C/T snv 0.32 7
rs1057519743
CRLF2
0.827 0.120 Y 1196852 missense variant A/C snv 6
rs2413739
PACSIN2
0.827 0.120 22 43001030 intron variant C/T snv 0.43 6
rs724159947
ETV6
0.851 0.120 12 11869601 missense variant C/T snv 6
rs9479
PML
0.851 0.120 15 74036235 3 prime UTR variant A/G snv 0.50 6
rs1057519866
NT5C2
0.851 0.120 10 103093198 missense variant C/T snv 5
rs6021191
NFATC2
0.851 0.120 20 51419700 intron variant A/T snv 4.9E-02 5
rs7853758
LOC105376116 ; SLC28A3
0.851 0.120 9 84286011 synonymous variant G/A snv 0.15 0.19 5
rs17007695 0.851 0.120 4 141788570 intergenic variant T/C snv 7.7E-02 4
rs17069665
FOXO3
0.882 0.120 6 108620265 intron variant A/C;G snv 4
rs4646450
CYP3A5 ; ZSCAN25
0.882 0.120 7 99668695 3 prime UTR variant G/A snv 0.38 4
rs4748793 0.851 0.120 10 22194082 intergenic variant A/G snv 0.18 4
rs6964969
IKZF1
0.851 0.120 7 50405553 downstream gene variant A/G snv 0.23 4
rs7088318
PIP4K2A
0.851 0.120 10 22564019 intron variant C/A snv 0.55 4
rs757874631
CBL
0.882 0.120 11 119278211 missense variant T/A;C snv 4
rs757891309
MTR
0.882 0.120 1 236850389 missense variant C/A;T snv 4.0E-06; 4.0E-06 4
rs7789635 0.882 0.120 7 50405912 downstream gene variant T/C snv 0.40 4
rs786205155
ETV6
0.882 0.120 12 11884481 missense variant T/C snv 4
rs9400241
FOXO3
0.882 0.120 6 108682786 3 prime UTR variant C/A;G snv 4
rs10235796
IKZF1
0.882 0.120 7 50394939 intron variant T/C snv 0.82 3
rs104893636
HOXD4 ; HOXD3
0.882 0.120 2 176151875 missense variant A/C;T snv 5.2E-06; 7.9E-04 3
rs1051296
SLC19A1
0.882 0.120 21 45514947 3 prime UTR variant A/C snv 0.43 0.44 3
rs10519612
IL15
0.882 0.120 4 141732548 intron variant A/C snv 0.10 3