Disease: Acute GVH disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs4553808
CTLA4
0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs749140677
VDR
0.752 0.240 12 47857185 missense variant G/A snv 8.0E-06 13
rs9277534
HLA-DPB1
0.790 0.280 6 33087030 3 prime UTR variant A/G snv 0.38 7
rs4693608
HPSE
0.827 0.200 4 83320204 intron variant G/A;C snv 6
rs4845618
IL6R
0.851 0.160 1 154427539 intron variant G/T snv 0.53 5
rs2278293
IMPDH1
0.882 0.040 7 128400698 non coding transcript exon variant C/T snv 0.47 3
rs7588571
REG3A
0.882 0.040 2 79161461 intron variant G/A snv 0.49 3
rs17114808
SUFU
0.925 0.040 10 102631528 3 prime UTR variant C/A;G;T snv 2