Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2395157
TSBP1-AS1
0.827 0.240 6 32380368 intron variant A/G snv 0.24 5
rs1701704
LOC105369781 ; IKZF4
0.851 0.200 12 56018703 intron variant T/G snv 0.25 5
rs3115553
TSBP1-AS1
0.851 0.200 6 32278050 intron variant C/T snv 0.25 4
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 9
rs574087
LOC102723878
1.000 0.040 11 64335476 upstream gene variant A/G snv 0.28 1
rs7682241 1.000 0.040 4 122602720 regulatory region variant G/T snv 0.30 1
rs485774
TSBP1-AS1 ; TSBP1
0.925 0.120 6 32323177 intron variant A/G snv 0.42 0.33 3
rs4916209 1.000 0.040 1 173164350 intergenic variant G/A snv 0.33 1
rs3099624 1.000 0.040 1 11436937 intergenic variant C/T snv 0.34 1
rs9268528 0.851 0.280 6 32415331 regulatory region variant A/G snv 0.34 4
rs3862469
CLEC16A
1.000 0.040 16 11100223 intron variant C/T snv 0.35 1
rs9479482 1.000 0.040 6 150036876 downstream gene variant T/C snv 0.36 1
rs7099812
MALRD1
1.000 0.040 10 19689469 intron variant T/G snv 0.41 1
rs405875 0.925 0.120 6 32247411 intergenic variant T/C snv 0.42 2
rs2216164
IFNG-AS1
1.000 0.040 12 68140560 intron variant A/G snv 0.49 1
rs9275141 0.827 0.240 6 32683340 intergenic variant T/G snv 0.50 6
rs9864529
LPP
1.000 0.040 3 188387268 intron variant G/A snv 0.52 2
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 7
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs12348691
PTCSC2
0.925 0.120 9 97846400 intron variant G/A snv 0.63 2
rs2292239
ERBB3
0.742 0.480 12 56088396 intron variant T/G snv 0.65 13
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs848
IL13 ; TH2LCRR
0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 8