Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1917799 0.851 0.120 10 49542929 upstream gene variant A/C snv 0.25 4
rs1002765
CHMP2B ; MIR4795
0.851 0.080 3 87227912 intron variant G/A;C snv 4
rs158572
ERCC8 ; NDUFAF2
0.851 0.120 5 60943616 intron variant G/A snv 0.63 4
rs121224
MIR365B ; MIR4725
0.851 0.080 17 31574981 intron variant G/C snv 0.66 4
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
rs6458238
PGC
0.882 0.080 6 41749967 intron variant G/A;C snv 4
rs2301756
PTPN11
0.851 0.120 12 112452972 intron variant A/G snv 0.21 4
rs9981660 0.882 0.080 21 42317828 upstream gene variant G/A snv 0.11 3
rs2029298
DDB2
0.882 0.080 11 47213167 upstream gene variant C/T snv 0.62 3
rs326222
DDB2
0.882 0.080 11 47238117 intron variant T/C snv 0.60 0.58 3
rs3781619
DDB2
0.882 0.080 11 47233766 intron variant G/A snv 0.26 3
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
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
rs7521584
MIR429
1.000 0.040 1 1168578 upstream gene variant T/A;G snv 3
rs158916
NDUFAF2
0.882 0.080 5 60949318 intron variant A/G snv 0.15 3
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
rs3814896
TFF2 ; LOC105372815
0.882 0.080 21 42351602 upstream gene variant A/G snv 0.17 3
rs10505799 1.000 0.040 12 16293334 intergenic variant T/C snv 0.10 2
rs6878265 1.000 0.040 5 120069960 intergenic variant C/T snv 0.29 2
rs1042194
CYP2C18
1.000 0.040 10 94735727 3 prime UTR variant G/C;T snv 2
rs2920283
JRK ; PSCA
0.925 0.040 8 142675619 intron variant T/C snv 0.44 2