Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800683
LOC100287329 ; LTA
0.807 0.240 6 31572294 5 prime UTR variant G/A;C snv 0.39 6
rs2072633
CFB ; CYP21A2 ; NELFE
0.807 0.320 6 31951801 3 prime UTR variant A/G snv 0.59 6
rs2509049
H2AX
0.827 0.160 11 119095811 upstream gene variant C/A;T snv 6
rs2844484
LTA ; LOC100287329
0.807 0.320 6 31568447 upstream gene variant A/G snv 0.64 6
rs3660
KRT86 ; KRT81
0.882 0.160 12 52286153 3 prime UTR variant C/G snv 0.51 6
rs3733846
CARMN
0.807 0.200 5 149425059 non coding transcript exon variant T/C snv 0.19 6
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 6
rs6449182
CD38
0.807 0.160 4 15778830 intron variant C/G snv 0.22 6
rs2069812
IL5
0.851 0.240 5 132544224 intron variant A/G snv 0.54 5
rs2070673
LOC107984284 ; CYP2E1
0.827 0.160 10 133527063 non coding transcript exon variant A/T snv 0.67 5
rs4833103
TLR1
0.925 0.160 4 38813881 intron variant A/C snv 0.64 5
rs1053667
TOGARAM1
0.925 0.120 14 45073835 3 prime UTR variant T/C snv 0.11 4
rs11337
GOLGA7
0.925 0.120 8 41510767 3 prime UTR variant T/G snv 0.93 4
rs113686495
CASP8
0.925 0.160 2 201258757 intron variant ATTCTGTC/- delins 4
rs1353759920
TP73
0.851 0.120 1 3707593 missense variant C/A snv 2.1E-05 4
rs3769821
CASP8
0.851 0.200 2 201258707 intron variant C/T snv 0.57 4
rs4150506
ERCC3
0.851 0.120 2 127262970 intron variant G/A snv 0.18 4
rs537160
CYP21A2 ; CFB
0.882 0.240 6 31948623 intron variant A/G snv 0.73 4
rs1041163
VCAM1
0.882 0.160 1 100718269 upstream gene variant T/C snv 0.18 3
rs11038689
CRY2
0.882 0.160 11 45852713 intron variant A/G snv 0.19 3
rs1401417
CRY2
0.882 0.160 11 45858559 intron variant C/G snv 0.19 3
rs227060
C11orf65 ; ATM
0.882 0.160 11 108334154 intron variant C/T snv 0.27 3
rs2857597
AIF1
0.882 0.200 6 31617223 upstream gene variant T/A snv 0.74 3
rs3115667 0.882 0.200 6 31675622 downstream gene variant T/A;C snv 0.74 3
rs4901706
TMEM260
1.000 0.120 14 56647667 3 prime UTR variant G/A;C;T snv 3