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
rs3025058
MMP3
0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs28360317
XRCC4
0.716 0.280 5 83323739 intron variant -/CCT delins 0.24 15
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins 11
rs1205454520
KLLN ; PTEN
0.763 0.120 10 87864059 5 prime UTR variant -/G delins 7.2E-06 10
rs11453459
PPP2R1A
0.882 0.080 19 52189696 upstream gene variant -/G delins 3
rs10680577
RAB4B-EGLN2 ; EGLN2
0.776 0.160 19 40798690 intron variant -/TACT delins 10
rs144848
BRCA2
0.653 0.440 13 32332592 missense variant A/C snv 0.28 0.23 29
rs712
KRAS
0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs735482
CD3EAP ; ERCC1
0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs12951053
TP53
0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs1057519697
ALK
0.776 0.120 2 29220830 missense variant A/C snv 12
rs1105879
UGT1A9 ; UGT1A6 ; UGT1A7 ; UGT1A10 ; UGT1A8
0.790 0.240 2 233693556 missense variant A/C snv 0.35 0.34 11
rs1204382931
CYP1B1 ; CYP1B1-AS1
0.790 0.160 2 38075270 missense variant A/C snv 4.3E-06 10
rs17486278
CHRNA5
0.827 0.120 15 78575140 intron variant A/C snv 0.32 9
rs1057519729
MAP2K1
0.827 0.080 15 66435113 missense variant A/C snv 6
rs11137037
ANGPT2 ; MCPH1
0.851 0.200 8 6538661 intron variant A/C snv 0.40 4
rs2844337
PAK1
0.851 0.120 11 77322663 3 prime UTR variant A/C snv 0.28 4
rs425366
CHL1
0.851 0.080 3 283727 intron variant A/C snv 0.56 4
rs9554314
FLT1
0.851 0.080 13 28301652 3 prime UTR variant A/C snv 4
rs1043973338
IL1B
0.882 0.080 2 112830483 missense variant A/C snv 3
rs188912830
MIR3202-1 ; MIR3202-2 ; TMEM187
0.882 0.080 X 153981098 non coding transcript exon variant A/C snv 3
rs4713354
MDC1
0.882 0.080 6 30717643 upstream gene variant A/C snv 0.22 3
rs7109645
PAK1
0.882 0.080 11 77475278 non coding transcript exon variant A/C snv 0.29 3
rs7248167 0.882 0.080 19 43455962 downstream gene variant A/C snv 0.22 3