Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs765803011
IL4R
1.000 0.040 16 27363094 missense variant C/G;T snv 4.0E-06; 1.6E-05 1
rs2920283
JRK ; PSCA
0.925 0.040 8 142675619 intron variant T/C snv 0.44 2
rs9315542
LINC00571 ; LINC02334
1.000 0.040 13 38057334 intron variant T/C snv 0.26 1
rs61516247
LINC00951 ; TDRG1
1.000 0.040 6 40344500 non coding transcript exon variant G/A snv 0.17 1
rs6672420
LOC105376878 ; RUNX3
0.827 0.120 1 24964519 missense variant A/T snv 0.56 0.50 6
rs1440526066
LOC105379176 ; IL4
1.000 0.040 5 132679827 missense variant G/A snv 1
rs629367
MIR100HG ; MIRLET7A2
0.776 0.200 11 122146306 intron variant C/A snv 0.88 11
rs6939861
MIR10398 ; TFEB
0.882 0.080 6 41735303 intron variant G/A snv 0.24 3
rs895819
MIR23A ; LOC284454 ; MIR27A ; MIR24-2
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs121224
MIR365B ; MIR4725
0.851 0.080 17 31574981 intron variant G/C snv 0.66 4
rs7521584
MIR429
1.000 0.040 1 1168578 upstream gene variant T/A;G snv 3
rs10739971
MIRLET7A1 ; MIRLET7F1
0.882 0.080 9 94175398 intron variant G/A;C snv 5
rs8111742
MIRLET7E ; MIR99B ; SPACA6 ; SPACA6P-AS ; MIR125A
0.851 0.120 19 51692221 intron variant G/A;C snv 0.30 4
rs17276588
MIRLET7F2 ; MIR98 ; HUWE1
0.882 0.120 X 53557457 intron variant G/A snv 9.0E-02 4.2E-02 4
rs2014486
MUC5B
1.000 0.040 11 1237573 intron variant A/G snv 0.52 2
rs7481521
MUC6
1.000 0.040 11 1027811 missense variant C/T snv 0.50 0.47 1
rs158916
NDUFAF2
0.882 0.080 5 60949318 intron variant A/G snv 0.15 3
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 30
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs9471643
PGC
0.882 0.080 6 41751177 intron variant G/C snv 0.19 6
rs6458238
PGC
0.882 0.080 6 41749967 intron variant G/A;C snv 4
rs3789210
PGC
0.882 0.080 6 41743584 intron variant C/G;T snv 3
rs4711690
PGC
0.882 0.080 6 41741200 missense variant C/G snv 0.19 0.20 3
rs6912200
PGC
0.925 0.080 6 41750170 intron variant C/T snv 0.54 3