Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs280519
TYK2
0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 10
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 13
rs12720270
TYK2
0.851 0.240 19 10365084 intron variant G/A snv 0.21 0.16 4
rs34725611
TYK2
1.000 0.080 19 10366391 intron variant A/G snv 0.28 0.23 1
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs280500
TYK2
0.882 0.200 19 10379726 5 prime UTR variant A/G snv 0.20 3
rs2255336
LOC101928100 ; KLRK1 ; KLRC4-KLRK1
0.827 0.200 12 10379727 missense variant T/C snv 0.81 0.74 5
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs1048257
PLD4 ; AHNAK2
1.000 0.080 14 104938047 3 prime UTR variant T/C;G snv 0.54 1
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs802791
ATG5
0.851 0.160 6 106121395 intron variant T/C snv 0.75 4
rs6568431
ATG5
0.790 0.320 6 106140931 intron variant A/C snv 0.61 7
rs9373839
ATG5
0.882 0.080 6 106207742 intron variant T/C snv 0.15 3
rs2299864
ATG5
1.000 0.080 6 106220119 intron variant C/T snv 0.15 1
rs3827644
ATG5
0.925 0.080 6 106237320 intron variant G/C snv 0.15 2
rs573775
ATG5
0.851 0.320 6 106316991 intron variant G/A snv 0.34 4
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs878859113
CD24
0.763 0.360 6 106971734 missense variant G/A snv 0.35 11
rs9514828
TNFSF13B
0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs12583006
TNFSF13B
0.807 0.320 13 108285104 intron variant T/A snv 0.21 8
rs7819602
LOC112268022
1.000 0.080 8 10869332 intergenic variant C/G;T snv 1
rs3087456
CIITA ; LOC105371080
0.742 0.480 16 10877045 intron variant G/A snv 0.53 14
rs4956211 1.000 0.080 4 108801970 intergenic variant G/A snv 0.37 1
rs6985109
XKR6
1.000 0.080 8 10904075 intron variant G/A;C;T snv 1