Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7765004 0.925 0.120 6 113750518 regulatory region variant A/C snv 0.32 2
rs777500092
DNMT3A
1.000 0.120 2 25246231 missense variant G/A snv 8.0E-06 2
rs931920092
EFS
0.925 0.120 14 23357350 missense variant G/A;C snv 2
rs201345298
PTPN6
1.000 0.120 12 6955413 missense variant C/A snv 3.8E-04 4.0E-04 1
rs2272990
RIPK1
1.000 0.120 6 3076907 missense variant T/C;G snv 0.91 1
rs2523607
HLA-B ; MIR6891
1.000 0.120 6 31355013 non coding transcript exon variant T/A snv 1
rs4733601 1.000 0.120 8 128257220 TF binding site variant A/G snv 0.41 1
rs6773363 1.000 0.120 3 27752141 intergenic variant T/A;C snv 1
rs79464052
ARAP3
1.000 0.120 5 141655607 intron variant G/C snv 7.1E-02 7.8E-02 1
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 11
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 6
rs6449182
CD38
0.807 0.160 4 15778830 intron variant C/G snv 0.22 6
rs116446171 0.851 0.160 6 484453 downstream gene variant C/G snv 2.3E-02 4
rs2425752
NCOA5
0.851 0.160 20 46073481 intron variant T/C snv 0.79 4
rs806321
DLEU1
0.851 0.160 13 50267187 intron variant C/T snv 0.47 4
rs1323292
LOC105371664
0.882 0.160 1 192571891 intron variant G/A snv 0.86 3
rs1444766
KALRN
0.882 0.160 3 124206424 intron variant A/G;T snv 3
rs41289586
ANO10
0.882 0.160 3 43577066 missense variant C/T snv 1.8E-02 1.9E-02 3
rs10462020
PER3
0.925 0.160 1 7820623 missense variant T/G snv 0.17 0.16 2
rs16978630
TNPO2
0.925 0.160 19 12702869 missense variant T/C;G snv 4.1E-02 2
rs79480871 0.925 0.160 2 24471603 intergenic variant C/T snv 9.3E-02 2
rs1057520009
XPO1
0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 14
rs1625895
TP53
0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06 13
rs1164376164
ABCB1
0.851 0.200 7 87601024 5 prime UTR variant A/G snv 6
rs1883112
NCF4-AS1 ; NCF4
0.851 0.200 22 36860804 intron variant G/A snv 0.39 4