Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2293157
STAT5A
0.763 0.120 17 42300657 intron variant C/A;T snv 9
rs1494555
IL7R
0.790 0.120 5 35871088 missense variant G/A snv 0.64 0.72 8
rs1057519825
BTK
0.882 0.120 X 101356176 missense variant C/G snv 7
rs1057519826
BTK
0.882 0.120 X 101356177 missense variant A/T snv 7
rs9392504 0.827 0.120 6 412802 downstream gene variant G/A snv 0.44 7
rs4985726
TNFRSF13B
0.925 0.120 17 16960324 intron variant C/G snv 0.11 5
rs11866002
CNOT1
0.851 0.120 16 58553833 synonymous variant C/T snv 0.35 0.39 4
rs3755397
FARP2
0.925 0.120 2 241355498 upstream gene variant A/G snv 6.8E-02 4
rs1057519831
PLCG2
1.000 0.120 16 81912655 missense variant C/T snv 3
rs139996880
TERT
0.882 0.120 5 1284538 intron variant G/A snv 0.12 3
rs210134
BAK1 ; GGNBP1
1.000 0.120 6 33572432 intron variant A/G snv 0.72 3
rs210142
GGNBP1 ; BAK1
0.925 0.120 6 33579060 intron variant T/C snv 0.74 3
rs2292982
IRF8
1.000 0.120 16 85911217 intron variant T/C;G snv 3
rs35923643
GRAMD1B
0.925 0.120 11 123484683 intron variant A/G snv 0.15 3
rs4987852
BCL2
0.925 0.120 18 63126688 3 prime UTR variant T/C snv 5.1E-02 3
rs9815073
LPP
0.925 0.120 3 188397894 intron variant C/A;G snv 3
rs1036935 0.925 0.120 18 50317164 upstream gene variant A/G;T snv 2
rs1044873
IRF8
0.925 0.120 16 85922065 3 prime UTR variant C/T snv 0.40 2
rs11636802
LOC105370831
0.925 0.120 15 56483399 intergenic variant A/G snv 8.0E-02 2
rs11637565
DRAIC
0.925 0.120 15 69728186 intron variant G/A snv 0.66 2
rs1274963
CSRNP1
0.925 0.120 3 39149538 non coding transcript exon variant A/G snv 0.82 2
rs13015798
FAM126B
0.925 0.120 2 201044792 intron variant A/G snv 0.23 2
rs13401811
ACOXL
0.925 0.120 2 110858527 intron variant G/A snv 0.19 2
rs1359742 0.925 0.120 9 22336997 intergenic variant G/C;T snv 2
rs1373425060
AK3
0.925 0.120 9 4719290 missense variant G/C snv 4.0E-06 2