Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs848
IL13 ; TH2LCRR
0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 8
rs3789129
ACOXL
1.000 0.040 2 110940463 intron variant A/C snv 0.18 1
rs4738296
KCNB2
1.000 0.040 8 72945304 upstream gene variant A/C snv 7.9E-02 1
rs6848139 1.000 0.040 4 122473886 intergenic variant A/C;G snv 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 9
rs2395157
TSBP1-AS1
0.827 0.240 6 32380368 intron variant A/G snv 0.24 5
rs111238176
FASLG
0.851 0.160 1 172665840 missense variant A/G snv 4
rs9268528 0.851 0.280 6 32415331 regulatory region variant A/G snv 0.34 4
rs485774
TSBP1-AS1 ; TSBP1
0.925 0.120 6 32323177 intron variant A/G snv 0.42 0.33 3
rs2216164
IFNG-AS1
1.000 0.040 12 68140560 intron variant A/G snv 0.49 1
rs574087
LOC102723878
1.000 0.040 11 64335476 upstream gene variant A/G snv 0.28 1
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 13
rs17031716
MAGI3
1.000 0.040 1 113609225 intron variant C/A snv 0.18 1
rs6906608
IRF4
1.000 0.040 6 411554 downstream gene variant C/A snv 0.11 1
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1800520
AIRE
0.851 0.200 21 44290023 missense variant C/A;G;T snv 0.14; 8.3E-06 5
rs6457452
HSPA1B
0.851 0.200 6 31827773 5 prime UTR variant C/G;T snv 8.5E-05; 9.3E-02; 1.4E-05 4
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs1057518972
TRPS1
0.827 0.200 8 115418359 missense variant C/T snv 7
rs3115553
TSBP1-AS1
0.851 0.200 6 32278050 intron variant C/T snv 0.25 4
rs10760706
STX17
1.000 0.040 9 99961410 intron variant C/T snv 0.69 1