Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs200349593
NXPE2 ; NXPE1
1.000 0.040 11 114526440 intron variant -/C;CCACTCTCTTCCTC ins 1
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs17780256
LOC105371887 ; SLC39A11
0.827 0.120 17 72646784 3 prime UTR variant A/C snv 0.18 6
rs10775412
KSR1
0.827 0.120 17 27542007 intron variant A/C snv 0.30 5
rs1517352
STAT4
0.851 0.160 2 191066738 intron variant A/C snv 0.45 5
rs1551399
LOC105375746
0.827 0.120 8 125527723 intron variant A/C snv 0.46 5
rs360718
IL18
0.827 0.120 11 112164016 5 prime UTR variant A/C snv 0.26 5
rs61802846
FCGR2A
0.827 0.120 1 161504083 upstream gene variant A/C snv 8.8E-02 5
rs72796353
NOD2
0.882 0.080 16 50712383 3 prime UTR variant A/C snv 1.3E-02 1.4E-02 5
rs3814057
NR1I2
0.925 0.040 3 119818407 3 prime UTR variant A/C snv 0.28 4
rs2382817
PNKD ; TMBIM1
0.925 0.040 2 218286495 5 prime UTR variant A/C snv 0.61 3
rs6017342
LINC01620
0.925 0.120 20 44436388 non coding transcript exon variant A/C snv 0.62 3
rs4598195
LOC105375444
1.000 0.040 7 107862996 intergenic variant A/C snv 0.34 1
rs7210086
SLC39A11 ; LOC105371887
1.000 0.040 17 72645559 downstream gene variant A/C snv 0.17 1
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs16910526
CLEC7A ; LOC105369655
0.742 0.280 12 10118488 stop gained A/C;G snv 6.2E-02 12
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 12
rs280519
TYK2
0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 10
rs714830
CDKAL1
0.827 0.120 6 20624151 intron variant A/C;G snv 0.13 5
rs7195296 0.827 0.120 16 11655918 intergenic variant A/C;G snv 5
rs2228055
IL10RA
0.851 0.280 11 117994131 missense variant A/C;G snv 8.2E-02 4
rs798502
AMZ1 ; GNA12
1.000 0.040 7 2750246 intron variant A/C;G snv 4
rs200711300
PTPN2
0.925 0.040 18 12802118 missense variant A/C;G snv 1.6E-04; 4.0E-06 3