Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333739
RAVER2
1 64827766 intron variant A/G;T snv 0.62 1
rs1889740
ARNT
1 150827279 intron variant C/T snv 0.42 1
rs2780889
RAVER2 ; JAK1
1 64833108 3 prime UTR variant A/T snv 0.52 1
rs765797019
PIK3CD
1 9720754 missense variant C/T snv 3.3E-05 3.5E-05 1
rs774263008
FCRL3
1 157697767 missense variant C/T snv 4.0E-06 1
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs17561
IL1A
0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26 23
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs114846446
LINC01250
0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs36001488
ATG16L1
0.724 0.240 2 233276621 intron variant C/T snv 0.44 14
rs3811047
IL37
0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 10
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs13003464
PUS10
0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs7568275
STAT4
0.827 0.120 2 191101726 intron variant G/C;T snv 6
rs11675342
TPO
0.851 0.040 2 1403856 intron variant C/T snv 0.40 5
rs13010713
LINC01934
0.882 0.200 2 181131318 intron variant A/C;G snv 5
rs1534430
MIR3681HG
0.851 0.040 2 12504610 intron variant C/T snv 0.35 5
rs17035378
PLEK ; LOC101927723
0.882 0.200 2 68371823 intron variant T/A;C snv 5
rs2075302
FAP
0.882 2 162219636 intron variant T/C snv 0.34 5