Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs861530
LOC112268131 ; XRCC3 ; KLC1
0.732 0.320 14 103707786 3 prime UTR variant T/C snv 0.65 13
rs2239633
CEBPE
0.742 0.240 14 23119848 upstream gene variant G/A snv 0.38 12
rs80338880
TFR2
0.732 0.360 7 100633100 stop gained G/C snv 7.0E-06 12
rs10821936
ARID5B
0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs213210
MIR219A1 ; RING1
0.742 0.240 6 33208047 upstream gene variant A/C;G snv 11
rs2536
MTOR
0.776 0.240 1 11106656 3 prime UTR variant T/C snv 5.8E-02 11
rs3824662
GATA3
0.752 0.320 10 8062245 intron variant C/A;T snv 11
rs1470755915
RUNX1T1
0.776 0.240 8 92005229 missense variant C/A snv 7.0E-06 10
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 10
rs3731217
CDKN2A
0.763 0.320 9 21984662 intron variant A/C;T snv 10
rs7089424
ARID5B
0.752 0.200 10 61992400 intron variant T/G snv 0.32 10
rs1057519753
JAK1
0.763 0.120 1 64846664 missense variant C/A snv 9
rs10828317
PIP4K2A
0.776 0.280 10 22550699 missense variant T/C snv 9
rs11978267
IKZF1
0.763 0.240 7 50398606 intron variant A/G snv 0.25 9
rs2069727
IFNG ; IFNG-AS1
0.763 0.320 12 68154443 intron variant T/A;C snv 9
rs4132601
IKZF1
0.763 0.240 7 50402906 3 prime UTR variant T/G snv 0.25 9
rs1966862
ARHGAP24
0.790 0.120 4 85766908 intron variant A/G snv 0.14 8
rs10740055
ARID5B
0.790 0.240 10 61958720 intron variant C/A snv 0.49 7
rs10994982
ARID5B
0.790 0.120 10 61950345 intron variant A/G snv 0.49 7
rs121913488
FLT3
0.807 0.120 13 28018505 missense variant C/A;G;T snv 7
rs3135388
HLA-DRA
0.807 0.240 6 32445274 downstream gene variant A/G snv 0.90 7
rs869312821
GNB1
0.882 0.120 1 1806515 missense variant T/C snv 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
rs210143
GGNBP1 ; BAK1
0.827 0.160 6 33579153 intron variant T/C snv 0.74 6