Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs4646903
CYP1A1
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs3742330
DICER1
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs937283
MDM2
0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19
rs2735383
OSGIN2 ; NBN
0.708 0.360 8 89935041 3 prime UTR variant C/G snv 0.31 18
rs1321311 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 15
rs1665650
HSPA12A
0.752 0.160 10 116727589 intron variant T/C snv 0.69 12
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 12
rs2494938
LRFN2
0.752 0.240 6 40568389 intron variant G/A snv 0.51 11
rs28366003
MT2A
0.763 0.240 16 56608579 upstream gene variant A/C;G snv 4.6E-02 10
rs59336
TBX3
0.776 0.160 12 114678547 intron variant T/A;G snv 0.49 10
rs115160714
TOPBP1
0.807 0.200 3 133601021 3 prime UTR variant G/A snv 5.8E-03 9
rs6877842
DROSHA ; C5orf22
0.807 0.320 5 31532531 intron variant G/C snv 0.16 7
rs13078
DICER1
0.827 0.280 14 95090410 3 prime UTR variant A/T snv 0.85 5
rs5744455
CD14 ; TMCO6
0.882 0.160 5 140633722 upstream gene variant G/A;T snv 5
rs11191865
STN1
0.925 0.160 10 103913084 intron variant G/A snv 0.44 3
rs9363918 0.882 0.200 6 68432116 intron variant T/G snv 0.38 3
rs10088262
LOC105375739
0.925 0.160 8 123753462 intergenic variant A/G snv 0.56 2
rs12765878
STN1
0.925 0.160 10 103909864 intron variant T/A;C snv 2
rs4725443
KMT2C
0.925 0.120 7 152170176 intron variant T/C snv 9.3E-02 2