Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs2274223
PLCE1
0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs879253942
TP53
0.677 0.400 17 7673826 missense variant A/G snv 28
rs3742330
DICER1
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs937283
MDM2
0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19
rs4711998
IL17A
0.708 0.360 6 52185555 upstream gene variant A/G snv 0.64 16
rs619586
MALAT1
0.724 0.360 11 65498698 non coding transcript exon variant A/G snv 5.9E-02 3.3E-02 15
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs2494752
AKT1
0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs3731239
CDKN2A
0.763 0.240 9 21974219 intron variant A/G snv 0.26 10
rs1834306
MIR10526 ; MIR100 ; MIR100HG
0.776 0.200 11 122152479 intron variant A/G snv 0.49 9
rs7023329
MTAP
0.790 0.160 9 21816529 intron variant A/G snv 0.50 9
rs1126667
ALOX12 ; ALOX12-AS1
0.776 0.280 17 6999441 missense variant A/G snv 0.60 0.62 8
rs1883965
MTOR
0.807 0.160 1 11262099 intron variant A/G snv 0.63 8
rs886205
ALDH2
0.827 0.360 12 111766623 intron variant A/G snv 0.35 8
rs13016963
FLACC1
0.851 0.080 2 201298088 intron variant A/G snv 0.59 5
rs2395655
CDKN1A ; DINOL
0.882 0.120 6 36677919 5 prime UTR variant A/G snv 0.43 0.49 5
rs10061133
MIR449B ; MIR449A ; CDC20B
0.851 0.160 5 55170716 mature miRNA variant A/G snv 0.11 8.6E-02 4
rs13182402
ALDH7A1
0.925 0.160 5 126582456 intron variant A/G snv 0.15 4
rs3219218
UNG
0.851 0.120 12 109100430 intron variant A/G snv 1.9E-02 4
rs11752942
LINC00951 ; TDRG1
0.882 0.080 6 40354019 intron variant A/G snv 0.46 3
rs1801426
BRCA2
0.882 0.120 13 32398747 missense variant A/G snv 2.3E-02 3.8E-02 3
rs2005618
MBD4
0.925 0.200 3 129432824 intron variant A/G snv 0.23 2