Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 10
rs1057519864
AR
0.851 0.080 X 67723707 missense variant T/C snv 8
rs976306779
AR
0.851 0.080 X 67545492 missense variant C/A;T snv 6.6E-06 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
rs137852581
AR
0.882 0.080 X 67723701 missense variant C/T snv 5
rs864622007
AR
0.882 0.200 X 67711621 missense variant T/A snv 5
rs17276588
MIRLET7F2 ; MIR98 ; HUWE1
0.882 0.120 X 53557457 intron variant G/A snv 9.0E-02 4.2E-02 4
rs8371
XIAP
0.925 0.120 X 123912065 3 prime UTR variant C/T snv 0.25 0.19 4
rs9856
XIAP
0.925 0.120 X 123911791 3 prime UTR variant C/T snv 0.57 4
rs111638916
PSMD10
0.925 0.080 X 108084839 3 prime UTR variant G/A snv 3
rs199469667
MED12
0.925 0.120 X 71119380 missense variant T/G snv 3
rs80291436
VCX
1.000 0.080 X 7843706 missense variant T/A;C;G snv 4.9E-05; 0.19 3
rs146462069
IGSF1
X 131278706 missense variant T/C;G snv 3.8E-05; 9.5E-03 2
rs1397372871
MED12
X 71119415 stop gained C/T snv 1
rs17216603
HEPH
X 66198947 missense variant G/A snv 2.4E-02 2.1E-02 1
rs3761624
TLR8 ; TLR8-AS1
X 12905562 intron variant A/G snv 0.29 1
rs6643869
PLS3
X 115597455 intron variant G/A snv 0.30 1
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs1065852
NDUFA6-DT ; LOC112268294 ; CYP2D6
0.695 0.360 22 42130692 missense variant G/A snv 0.21 0.19 19
rs2267437
DESI1 ; XRCC6
0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs1057519911
MAPK1
0.776 0.160 22 21772875 missense variant C/T snv 10
rs137853007
CHEK2
0.790 0.240 22 28725254 missense variant G/A;T snv 5.2E-05 9