Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs130555
SYN3
1.000 0.040 22 32787803 intron variant C/T snv 0.77 2
rs3116494
CD28
0.882 0.120 2 203727298 intron variant G/A snv 0.76 4
rs4552569 1.000 0.040 5 83877774 upstream gene variant C/T snv 0.75 2
rs3810936
TNFSF15
0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75 12
rs1861494
IFNG-AS1 ; IFNG
0.716 0.400 12 68157629 intron variant C/T snv 0.75 15
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13
rs17119
LOC101928354
0.882 0.120 6 14719265 intron variant G/A snv 0.74 4
rs564349
ERGIC1
5 172897975 3 prime UTR variant G/A snv 0.73 1
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 10
rs1648234
CSRP3-AS1
11 19308167 intron variant G/A snv 0.72 1
rs5743810
TLR6 ; TLR1
0.689 0.360 4 38828729 missense variant A/G snv 0.73 0.72 21
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2305767
MYO9B
0.882 0.280 19 17183487 intron variant C/T snv 0.70 4
rs6795970
SCN10A
0.807 0.200 3 38725184 missense variant A/G snv 0.65 0.70 13
rs2315008
ZGPAT
0.925 0.120 20 63712604 intron variant T/G snv 0.70 4
rs2695121
NR1H2
0.716 0.280 19 50377484 5 prime UTR variant T/C snv 0.70 16
rs6592362
LOC107984361
11 87414396 intergenic variant A/G snv 0.69 1
rs6142618
TM9SF4
20 32137845 intron variant A/G snv 0.69 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 9
rs4317455
PSMG4
6 3263257 intron variant C/T snv 0.68 1
rs449454
NDFIP1
0.925 0.080 5 142153497 3 prime UTR variant A/G snv 0.65 0.68 3
rs2228226
GLI1 ; ARHGAP9
0.851 0.160 12 57472038 missense variant G/C snv 0.60 0.68 6