Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs643434
ABO
9 133266942 intron variant A/G;T snv 8
rs75885714
PLCL2
3 16901018 intron variant A/C snv 4.6E-02 7
rs13412535
SERPINE2
2 224010157 intron variant G/A snv 0.17 5
rs61812598
IL6R
1.000 0.080 1 154447611 intron variant G/A snv 0.31 4
rs113600793
EFCAB13
17 47384095 intron variant C/A;T snv 3
rs12023396 1 231134890 intergenic variant A/G snv 0.21 2
rs12623456 2 163162632 intergenic variant T/C snv 2.2E-02 2
rs4749080 10 25873837 intergenic variant A/G snv 0.11 2
rs16838623
CHRM3
1 239648090 intron variant A/C snv 3.4E-02 2
rs17143586
ICA1
7 8137767 intron variant C/A snv 5.3E-02 2
rs7632000
ITPR1
3 4662253 intron variant C/G;T snv 1.3E-05; 4.0E-02 2
rs72831623
LOC112268184
17 47644927 intron variant G/A;C snv 4.0E-02 2
rs11627056
MDGA2
14 46985783 intron variant G/A snv 0.29 2
rs2823743
MIR99AHG
1.000 0.040 21 16295399 intron variant T/A;C snv 2
rs73273528 20 51814574 intergenic variant C/T snv 6.9E-02 1
rs7623146 3 63718309 intergenic variant G/A snv 0.15 1
rs146828618
KSR2
12 117570387 intron variant C/T snv 5.2E-03 1
rs196854
LOC112268023
8 24926467 intergenic variant C/T snv 0.89 1
rs781771
RNF220
1 44508410 intron variant T/A;C snv 1
rs4473152
SH2D7
15 78089318 intron variant C/G;T snv 1
rs4862562
SORBS2
4 185681056 intron variant A/C snv 0.10 1
rs113207090
TC2N
14 91793465 intron variant C/T snv 8.1E-03 1
rs6685273
VPS13D
1 12313691 intron variant C/T snv 5.7E-02 1
rs4986811
WT1
11 32429547 intron variant T/G snv 0.31 1