Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7270101
ITPA
0.776 0.200 20 3213247 intron variant A/C snv 8.7E-02 9.7E-02 10
rs7453920
HLA-DQB2
0.752 0.440 6 32762235 intron variant A/G;T snv 10
rs1993116
CYP2R1
0.827 0.200 11 14888688 intron variant A/G snv 0.65 8
rs910049
TSBP1-AS1 ; TSBP1
0.776 0.400 6 32347950 intron variant T/C snv 0.76 8
rs17401966
KIF1B
0.790 0.280 1 10325413 intron variant A/G snv 0.24 7
rs7944926
NADSYN1
0.807 0.200 11 71454579 intron variant A/G snv 0.54 7
rs893051
CLDN1
0.807 0.400 3 190321812 intron variant G/A;C snv 7
rs143633948
ARG1
0.882 0.080 6 131504454 intron variant G/A;C snv 6
rs1539019
NLRP3
0.882 0.240 1 247436999 intron variant A/C snv 0.63 6
rs2055979
IL21-AS1 ; IL21
0.827 0.320 4 122619586 intron variant C/A snv 0.23 6
rs2239185
VDR
0.807 0.320 12 47850776 intron variant G/A snv 0.54 6
rs35897606
KIAA1549L
0.882 0.080 11 33436311 intron variant A/G snv 4.4E-02 6
rs3764879
TLR8 ; TLR8-AS1
0.807 0.320 X 12906578 intron variant C/G snv 0.30 6
rs4074
CXCL1
0.827 0.200 4 73870427 intron variant A/G snv 0.46 6
rs73132848
CAV3 ; OXTR
0.882 0.080 3 8764738 intron variant G/A snv 9.3E-02 6
rs757343
VDR
0.807 0.360 12 47845892 intron variant C/T snv 0.12 6
rs1012068
DEPDC5
0.827 0.160 22 31869917 intron variant T/G snv 0.37 5
rs16851720
RNF7
0.827 0.120 3 141744456 intron variant A/C snv 0.21 5
rs17047200
TLL1
0.827 0.200 4 166008836 intron variant A/T snv 0.18 5
rs2596538
MICA ; MICA-AS1
0.851 0.160 6 31400855 intron variant G/A snv 0.41 5
rs5743314
TLR3
0.851 0.160 4 186079221 intron variant G/C;T snv 5
rs5998152
DEPDC5
0.827 0.160 22 31867176 intron variant T/C snv 0.37 5
rs11506105
EGFR
0.851 0.160 7 55152484 intron variant A/G snv 0.59 4
rs2267716
CRHR2
0.851 0.120 7 30677027 intron variant T/A;C snv 4
rs2305482
PSMD3
0.851 0.200 17 39984674 intron variant A/C snv 0.57 4