Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2029298
DDB2
0.882 0.080 11 47213167 upstream gene variant C/T snv 0.62 3
rs6912200
PGC
0.925 0.080 6 41750170 intron variant C/T snv 0.54 3
rs6878265 1.000 0.040 5 120069960 intergenic variant C/T snv 0.29 2
rs1886753
TDRG1
1.000 0.040 6 40359357 non coding transcript exon variant C/T snv 0.42 1
rs7481521
MUC6
1.000 0.040 11 1027811 missense variant C/T snv 0.50 0.47 1
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
rs3805246
GAB1
0.882 0.120 4 143382955 intron variant G/A snv 0.31 3
rs6939861
MIR10398 ; TFEB
0.882 0.080 6 41735303 intron variant G/A snv 0.24 3
rs9981660 0.882 0.080 21 42317828 upstream gene variant G/A snv 0.11 3
rs1440526066
LOC105379176 ; IL4
1.000 0.040 5 132679827 missense variant G/A snv 1
rs61516247
LINC00951 ; TDRG1
1.000 0.040 6 40344500 non coding transcript exon variant G/A snv 0.17 1
rs764097618
IL4R
1.000 0.040 16 27360794 splice donor variant G/A snv 4.0E-06 1
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
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
rs9471643
PGC
0.882 0.080 6 41751177 intron variant G/C snv 0.19 6