Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3781619
DDB2
0.882 0.080 11 47233766 intron variant G/A snv 0.26 3
rs3789210
PGC
0.882 0.080 6 41743584 intron variant C/G;T snv 3
rs3814896
TFF2 ; LOC105372815
0.882 0.080 21 42351602 upstream gene variant A/G snv 0.17 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
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
rs6672420
LOC105376878 ; RUNX3
0.827 0.120 1 24964519 missense variant A/T snv 0.56 0.50 6
rs830083
DDB2
0.807 0.120 11 47232500 intron variant G/A;C;T snv 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
rs1917799 0.851 0.120 10 49542929 upstream gene variant A/C snv 0.25 4
rs2301756
PTPN11
0.851 0.120 12 112452972 intron variant A/G snv 0.21 4
rs8111742
MIRLET7E ; MIR99B ; SPACA6 ; SPACA6P-AS ; MIR125A
0.851 0.120 19 51692221 intron variant G/A;C snv 0.30 4
rs3805246
GAB1
0.882 0.120 4 143382955 intron variant G/A snv 0.31 3
rs2607775
XPC ; LSM3
0.807 0.160 3 14178595 5 prime UTR variant C/G snv 0.42 0.43 8
rs629367
MIR100HG ; MIRLET7A2
0.776 0.200 11 122146306 intron variant C/A snv 0.88 11
rs6498486
ERCC4
0.776 0.200 16 13919809 upstream gene variant A/C snv 0.27 8
rs121434254
AIRE
0.807 0.200 21 44289773 stop gained C/A;T snv 7.5E-04 6
rs760805
RUNX3 ; LOC107984932
0.776 0.240 1 24925432 intron variant A/T snv 0.42 9
rs12229892
PTPN11
0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 6
rs11536878
TLR4
0.827 0.240 9 117709275 intron variant C/A snv 9.5E-02 5
rs2094258
ERCC5 ; BIVM-ERCC5
0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
rs2294008
PSCA ; JRK
0.672 0.320 8 142680513 5 prime UTR variant C/T snv 0.46 0.45 28
rs10983755 0.790 0.320 9 117702392 upstream gene variant G/A snv 3.2E-02 7