Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17103265
NFKBIA
0.925 0.080 14 35405503 upstream gene variant A/- delins 3
rs17109928
NOC3L
0.882 0.080 10 94338336 intron variant T/C;G snv 0.15 3
rs199971565
MIR302A ; MIR302D ; MIR302CHG ; MIR302C ; LARP7 ; MIR367 ; MIR302B
0.925 0.080 4 112648384 mature miRNA variant ACTT/- delins 2.1E-02 3
rs2029298
DDB2
0.882 0.080 11 47213167 upstream gene variant C/T snv 0.62 3
rs2057314
DCBLD1
0.882 0.080 6 117498194 intron variant A/G snv 0.61 3
rs2172362
LOC105378667
0.925 0.080 1 39829228 intergenic variant T/C snv 0.58 3
rs2293035
XRCC1
0.882 0.080 19 43546923 synonymous variant G/A snv 1.6E-04 1.5E-04 3
rs2294693
UNC5CL ; OARD1
1.000 0.080 6 41037763 intron variant T/C snv 0.26 3
rs230310
TRIT1
0.925 0.080 1 39842047 intron variant A/G;T snv 3
rs2515401
IL36RN
0.882 0.080 2 113062899 3 prime UTR variant T/A;C snv 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
rs2689154 0.882 0.080 1 238745053 intergenic variant C/A;G;T snv 3
rs3180235
IL36RN
0.882 0.080 2 113063095 3 prime UTR variant A/G snv 0.65 3
rs326222
DDB2
0.882 0.080 11 47238117 intron variant T/C snv 0.60 0.58 3
rs3738708
PARP1
0.925 0.080 1 226402338 missense variant G/A;C snv 7.0E-06 3
rs3761376
TFF1
0.925 0.080 21 42366929 upstream gene variant G/A snv 0.27 3
rs377566281
XRCC1
0.925 0.080 19 43552083 missense variant C/T snv 5.6E-05 2.1E-05 3
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
rs461404
PRKAA1
0.925 0.080 5 40799438 upstream gene variant G/A snv 0.70 3
rs4635002
DOCK1
0.925 0.080 10 127064415 intron variant A/C snv 0.92 3
rs4646421
CYP1A1
0.882 0.080 15 74723851 intron variant G/A;C;T snv 0.21 3
rs4711690
PGC
0.882 0.080 6 41741200 missense variant C/G snv 0.19 0.20 3
rs526934
TCN1
0.925 0.080 11 59866020 intron variant G/A snv 0.77 3