Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61 8
rs2665390
LOC107986148 ; TIPARP
0.776 0.160 3 156679960 intron variant C/T snv 0.92 8
rs3024971
STAT6
0.827 0.200 12 57099944 intron variant T/G snv 7.8E-02 7.9E-02 7
rs3176352
CDKN1A
0.807 0.120 6 36684562 intron variant C/A;G;T snv 8.0E-06; 0.37; 2.0E-05 7
rs34214448
NME1 ; NME1-NME2
0.851 0.120 17 51154651 intron variant G/T snv 0.39 7
rs3765459
CD40
0.807 0.280 20 46128768 intron variant G/A;C snv 0.22 7
rs4851527
IL1R2
0.790 0.160 2 102005914 intron variant A/G snv 0.63 7
rs7372209
CTDSPL ; MIR26A1
0.807 0.160 3 37969217 intron variant T/C snv 0.77 7
rs1266828
IL17F
0.807 0.120 6 52243264 intron variant G/A snv 0.75 6
rs13117307
EXOC1
0.827 0.080 4 55885574 intron variant C/T snv 0.21 6
rs3218896
IL1R2
0.807 0.160 2 102015190 intron variant T/C;G snv 6
rs4282438
COL11A2P1
0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 6
rs4848320
PAX8 ; PAX8-AS1
0.807 0.120 2 113253214 intron variant C/G;T snv 6
rs1143630
IL1B
0.827 0.160 2 112834078 intron variant T/A;G snv 5
rs11568785
TGFBR1
0.882 0.080 9 99143552 intron variant A/G;T snv 7.2E-02 5
rs266085
CXCL12
0.851 0.200 10 44378805 intron variant C/T snv 0.32 5
rs3826392
ZNF18 ; MAP2K4
0.827 0.200 17 12019587 intron variant G/T snv 0.65 5
rs719250
IL1R2
0.827 0.200 2 102007256 intron variant C/T snv 0.11 5
rs1007541
FSHR
0.882 0.080 2 48981895 intron variant C/T snv 0.16 4
rs1474348
IL6-AS1 ; IL6
0.882 0.080 7 22728289 intron variant C/G snv 0.71 4
rs16970849
TMC8
0.882 0.080 17 78137827 intron variant G/A;T snv 0.11; 4.0E-06 4
rs2289937
RAD21
0.882 0.080 8 116861572 intron variant G/A;C snv 4
rs2290907
TNRC6C
0.882 0.080 17 78097596 intron variant T/C snv 0.23 4
rs3809728
MAP2K4 ; ZNF18
0.851 0.120 17 12019847 intron variant A/C;T snv 4
rs4579555
RAD21
0.882 0.080 8 116867092 intron variant A/G snv 4