Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4833095
TLR1
0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 28
rs326222
DDB2
0.882 0.080 11 47238117 intron variant T/C snv 0.60 0.58 3
rs10505799 1.000 0.040 12 16293334 intergenic variant T/C snv 0.10 2
rs2920283
JRK ; PSCA
0.925 0.040 8 142675619 intron variant T/C snv 0.44 2
rs12423190
PTPN11
1.000 0.040 12 112471536 intron variant T/C snv 8.7E-02 1
rs9315542
LINC00571 ; LINC02334
1.000 0.040 13 38057334 intron variant T/C snv 0.26 1
rs7521584
MIR429
1.000 0.040 1 1168578 upstream gene variant T/A;G snv 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
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs1042194
CYP2C18
1.000 0.040 10 94735727 3 prime UTR variant G/C;T snv 2
rs9471643
PGC
0.882 0.080 6 41751177 intron variant G/C snv 0.19 6
rs121224
MIR365B ; MIR4725
0.851 0.080 17 31574981 intron variant G/C snv 0.66 4
rs830083
DDB2
0.807 0.120 11 47232500 intron variant G/A;C;T snv 6
rs254942
ERCC4
0.882 0.080 16 13932150 splice region variant G/A;C;T snv 0.97; 4.0E-06; 4.0E-06 3
rs10739971
MIRLET7A1 ; MIRLET7F1
0.882 0.080 9 94175398 intron variant G/A;C snv 5
rs1002765
CHMP2B ; MIR4795
0.851 0.080 3 87227912 intron variant G/A;C snv 4
rs6458238
PGC
0.882 0.080 6 41749967 intron variant G/A;C snv 4
rs8111742
MIRLET7E ; MIR99B ; SPACA6 ; SPACA6P-AS ; MIR125A
0.851 0.120 19 51692221 intron variant G/A;C snv 0.30 4
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 30
rs873601
BIVM-ERCC5 ; ERCC5
0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs10983755 0.790 0.320 9 117702392 upstream gene variant G/A snv 3.2E-02 7
rs12229892
PTPN11
0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 6
rs158572
ERCC8 ; NDUFAF2
0.851 0.120 5 60943616 intron variant G/A snv 0.63 4
rs17276588
MIRLET7F2 ; MIR98 ; HUWE1
0.882 0.120 X 53557457 intron variant G/A snv 9.0E-02 4.2E-02 4
rs3781619
DDB2
0.882 0.080 11 47233766 intron variant G/A snv 0.26 3