Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs393152
LINC02210 ; LINC02210-CRHR1
0.851 0.160 17 45641777 non coding transcript exon variant A/G snv 0.18 0.29 7
rs4979462
TNFSF15
0.790 0.240 9 114804733 intron variant C/T snv 0.13 7
rs683369
SLC22A1
0.807 0.360 6 160130172 missense variant G/A;C;T snv 4.0E-06; 0.83; 4.0E-06 7
rs7775055 0.790 0.200 6 32690139 TF binding site variant T/C snv 6.2E-02 7
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 7
rs919462
MAPT
0.807 0.120 17 45988374 intron variant C/T snv 0.15 7
rs11117433 0.827 0.160 16 85985910 upstream gene variant G/A;C;T snv 6
rs121434254
AIRE
0.807 0.200 21 44289773 stop gained C/A;T snv 7.5E-04 6
rs1234313
TNFSF4
0.807 0.400 1 173197108 intron variant A/G snv 0.72 6
rs1256030
ESR2
0.827 0.240 14 64280452 intron variant A/G;T snv 6
rs16841904
DENND1B
0.807 0.160 1 197732862 intron variant C/T snv 0.18 6
rs1864325
MAPT
0.882 0.160 17 45900461 intron variant C/T snv 0.14 6
rs35736272
ZPBP2
0.807 0.160 17 39876427 intron variant T/C snv 0.35 6
rs3757387
IRF5
0.851 0.280 7 128936032 upstream gene variant T/C snv 0.38 6
rs3784099
RAD51B
0.807 0.320 14 68283210 intron variant G/A snv 0.43 6
rs3807307
IRF5
0.827 0.120 7 128939148 intron variant T/C snv 0.41 6
rs4065275
ORMDL3
0.807 0.160 17 39924612 intron variant A/G;T snv 0.56 6
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 6
rs6974491
ELMO1
0.807 0.120 7 37334906 intron variant G/A snv 0.14 6
rs7665090
MANBA
0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 6
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 6
rs907091
IKZF3
0.851 0.280 17 39765489 3 prime UTR variant C/T snv 0.47 6
rs10445308
IKZF3
0.851 0.240 17 39781794 intron variant C/T snv 0.38 5
rs11557467
ZPBP2
0.851 0.200 17 39872381 missense variant G/T snv 0.45 0.45 5
rs12185268
MAPT-AS1 ; SPPL2C
0.851 0.160 17 45846317 missense variant A/G snv 0.15 0.14 5